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Torsten Passie

Hannover Medical School, Hannover, Germany.

31 papers in the library · 3,017 citations · publishing 2002-2025

Papers

Safety and Efficacy of Lysergic Acid Diethylamide-Assisted Psychotherapy for Anxiety Associated With Life-threatening Diseases

The Journal of Nervous and Mental Disease March 4, 2014 Peter Gasser, Dominique Holstein, Yvonne Michel et al. 752 citations

In a small pilot study, 12 patients with anxiety related to life-threatening diseases underwent two sessions of LSD-assisted psychotherapy, receiving either a full 200-microgram dose or a low 20-microgram active placebo, with the placebo group later crossing over to the full dose. At a 2-month follow-up, trait anxiety decreased with a large effect size, and state anxiety also dropped significantly. These anxiety reductions persisted for 12 months. No serious adverse effects occurred beyond one day after treatment. The findings suggest that, under careful medical supervision, LSD can reduce anxiety, supporting the need for larger controlled trials.

The pharmacology of psilocybin

Addiction Biology October 1, 2002 Torsten Passie, Juergen Seifert, Udo Schneider et al. 465 citations

Psilocybin, the main psychoactive alkaloid in certain mushrooms found worldwide, is increasingly abused as a hallucinogenic drug. Although it was used experimentally in medicine during the 1960s, pharmacological information about it remained scarce until recently. This review compiles all available pharmacological data on psilocybin, addressing the ongoing abuse potential and the need for comprehensive knowledge.

The Pharmacology of Lysergic Acid Diethylamide: A Review

CNS Neuroscience & Therapeutics November 11, 2008 Torsten Passie, John H. Halpern, Dirk O. Stichtenoth et al. 459 citations

Lysergic acid diethylamide (LSD) was synthesized in 1938 and its psychoactive effects discovered in 1943. It was used in psychiatric research during the 1950s and 1960s to produce experimental psychosis and in psycholytic and psychedelic therapy. After becoming an illegal drug of abuse from the mid-1960s, scientific interest has resumed with new methods and oversight. This review covers all aspects of LSD's pharmacology and psychopharmacology, based on nearly 10,000 scientific papers. LSD is physiologically well tolerated and psychological reactions can be controlled in a medical setting, but uncontrolled use risks complications. New interest focuses on LSD as a tool for studying consciousness and potential treatments for cluster headache and terminally ill patients.

LSD-assisted psychotherapy for anxiety associated with a life-threatening disease: A qualitative study of acute and sustained subjective effects

Journal of Psychopharmacology November 11, 2014 Peter Gasser, Katharina Kirchner, Torsten Passie 458 citations

In patients with anxiety linked to life-threatening diseases, LSD-assisted psychotherapy produced lasting benefits. Twelve months after treatment, none of the ten participants reported adverse reactions, and significant reductions in anxiety (measured by the STAI) were sustained. Qualitative interviews revealed that most participants experienced insightful, cathartic, and interpersonal encounters; 77.8% reported reduced anxiety and 66.7% reported improved quality of life. Subjective accounts pointed to facilitated access to emotions, confrontation of unknown anxieties and resources, and intense peak experiences as key psychological mechanisms. These experiences helped restructure emotional trust, situational understanding, habits, and worldview. The findings suggest that medically supervised LSD therapy can be safe and yield enduring benefits.

Reviewing the Potential of Psychedelics for the Treatment of PTSD

The International Journal of Neuropsychopharmacology March 12, 2020 Erwin Krediet, Tijmen Bostoen, Joost J. Breeksema et al. 262 citations

Posttraumatic stress disorder (PTSD) often remains chronic after psychotherapy, and few effective medications exist. A promising new approach involves psychedelic drugs. This review discusses four compound types: MDMA, ketamine, classical psychedelics (psilocybin, LSD), and cannabinoids. It describes each compound's therapeutic rationale, administration setting, and current evidence for treating PTSD. Each offers unique qualities, from rapidly targeting symptoms to facilitating psychotherapy. The review outlines questions for future research.

The early use of MDMA (‘Ecstasy’) in psychotherapy (1977–1985)

Drug Science Policy and Law January 1, 2018 Torsten Passie 115 citations

MDMA, also known as ecstasy, was first made in 1912 but became popular as a legal substitute for the illegal recreational drug MDA in 1970. Between 1977 and 1985, while still legal, a few dozen psychotherapists in the United States used MDMA for its benign, feeling-enhancing, and nonhallucinatory properties. This article examines the contexts and practices of that psychotherapeutic use. Some guidelines and precautions developed then are similar to those for psychedelic drugs, while others are specific to MDMA. The pioneering therapists developed techniques for individual and group therapy that laid the groundwork for later scientific studies, and the perceived beneficial effects of MDMA helped revive psycholytic/psychedelic therapy internationally.

The non-hallucinogen 2-bromo-lysergic acid diethylamide as preventative treatment for cluster headache: An open, non-randomized case series

Cephalalgia March 26, 2010 Matthias Karst, John H. Halpern, Michael Bernateck et al. 104 citations

Cluster headache is a severe, one-sided headache condition affecting 0.1% of people. Standard treatments like oxygen and sumatriptan can fail, and surgical options carry serious risks. An internet survey of 53 patients suggested that the hallucinogens psilocybin and LSD may abort attacks and extend remission better than standard drugs, but these substances are criminalized. To test whether a non-hallucinogenic LSD analog could also help, researchers investigated 2-bromo-LSD (BOL-148). Past studies found BOL-148 non-toxic and non-hallucinogenic, with only mild side effects at the dose used, and no long-term effects in over 300 healthy subjects or in schizophrenic women given 30mg daily for weeks.

Lower-dose psycholytic therapy – A neglected approach

Frontiers in Psychiatry December 2, 2022 Torsten Passie, Jeffrey Guss, Rainer Krähenmann 71 citations

Lysergic acid diethylamide (LSD) and similar psychoactive drugs have been used in psychotherapy since 1949, when the first clinical study with lower-dose LSD showed therapeutically relevant effects. Psycholytic therapy, named in 1960, involved serial lower-dose LSD or psilocybin sessions within a psychoanalytical framework, conducted in clinical settings on both inpatient and outpatient bases. Over 15 years, it was established at 30 clinical treatment centers and by more than 100 outpatient psychotherapists in Europe, while North America favored high-dose psychedelic therapy. Professor Hanscarl Leuner in Germany was the leading figure, providing a detailed analysis of the LSD reaction in a 1962 monograph. The article reviews evidence for psycholytic therapy's efficacy and argues for its inclusion in substance-assisted psychotherapy.

Rediscovering MDMA (ecstasy): the role of the American chemist Alexander T. Shulgin

Addiction August 1, 2010 Udo Benzenhöfer, Torsten Passie 69 citations

Alexander Shulgin is often called the 'father' of MDMA, but a re-assessment of his original publications and laboratory notebook shows he did not synthesize or try MDMA in 1965 as his book PIHKAL suggests. He learned of its special effects in the mid-1970s, re-synthesized it, and first tried it in September 1976. In 1977 he gave MDMA to psychotherapist Leo Zeff, who then introduced it to other therapists. Shulgin also co-authored the first paper on MDMA's pharmacological action in humans in 1978. These contributions explain why he is sometimes erroneously called the 'father' of MDMA, though he was not the first to synthesize it.

The History of MDMA as an Underground Drug in the United States, 1960–1979

Journal of Psychoactive Drugs March 3, 2016 Torsten Passie, Udo Benzenhöfer 56 citations

MDMA, also known as ecstasy, was first synthesized in 1912 and later resynthesized for pharmaceutical reasons before becoming a popular recreational drug. Drawing on previously overlooked U.S. government documents, this article traces MDMA's early recreational history in the U.S. from 1960 to 1979. MDMA appeared as a street drug in the late 1960s, with the first forensic detection in 1970 in Chicago. Underground chemists likely synthesized it as a legal alternative to MDA, which was scheduled under the Controlled Substances Act in 1970. Until 1974, nearly all seized MDMA street samples came from the U.S. Midwest, the first hot region of use. In Canada, MDMA was first detected in 1974 and scheduled in 1976.

MDA, MDMA, and other “mescaline‐like” substances in the US military's search for a truth drug (1940s to 1960s)

Drug Testing and Analysis August 29, 2017 Torsten Passie, Udo Benzenhöfer 43 citations

From the 1940s to the 1960s, the United States military explored mescaline and related compounds such as MDA, MDMA, and MDE as potential truth drugs for interrogation and behavior manipulation, following earlier German tests with mescaline. After animal testing, some derivatives were given to patients at the New York State Psychiatric Institute. During tests in 1952–53, an unwitting patient died, a fact kept secret. Subsequent secret animal studies in 1953–54 identified several mescaline derivatives for further human testing. By 1955, military focus shifted to LSD, though interest in mescaline-like compounds persisted for their ability to alter mood and habit without disrupting cognition. Whether any were used operationally remains unclear but probable.

A phenomenology of subjectively relevant experiences induced by ayahuasca in Upper Amazon vegetalismo tourism

Journal of Psychedelic Studies March 29, 2019 Tom Wolff, Simon Ruffell, Nigel Netzband et al. 41 citations

In a study of nine foreign tourists at an ayahuasca retreat in Peru, the typical structure of spontaneously reported experiences included personal preparation, physical symptoms, visual phenomena, cognitive and emotional phenomena, reactions within the psychedelic world and ordinary reality, and appraisal of the process. Emotional reactions ranged from pleasant (psychotherapeutic target emotions and hedonistic emotions) to unpleasant. For most participants, the presence of psychotherapeutic target emotions seemed to involve unpleasant emotions in the same session, possibly as transitional emotional states. This suggests psychodynamic processes, such as activation of emotional conflicts, can occur spontaneously during ayahuasca intake in this setting. Some participants attributed symbolic meaning to visionary content, more likely among psychotherapeutically motivated clients. The setting and expectations about native wisdom may influence experiences and interpretations.

Return of the lysergamides. Part VI: Analytical and behavioural characterization of 1‐cyclopropanoyl‐d‐lysergic acid diethylamide (1CP‐LSD)

Drug Testing and Analysis March 16, 2020 Simon D. Brandt, Pierce V. Kavanagh, Folker Westphal et al. 38 citations

1-Cylopropanoyl-LSD (1CP-LSD), a new lysergamide-based designer drug, was analyzed using multiple chemical and spectroscopic methods. Incubation with human serum converted 1CP-LSD into LSD, suggesting it may act as a prodrug for LSD in the body. In mice, 1CP-LSD induced a head-twitch response (HTR) with an ED50 of 430.0 nmol/kg, comparable to 1P-LSD (ED50 = 349.6 nmol/kg), indicating an LSD-like behavioral profile. The study includes analysis of blotters and pellets, and detected artificially induced degradation products during GC-MS analysis. Clinical studies are needed to determine its potency and effects in humans.

Validation of an LC-MS/MS method for the quantitative analysis of 1P-LSD and its tentative metabolite LSD in fortified urine and serum samples including stability tests for 1P-LSD under different storage conditions

Journal of Pharmaceutical and Biomedical Analysis May 28, 2019 Christina Grumann, Kerstin Henkel, Alexander Stratford et al. 27 citations

Psychedelics significantly alter urine metabolite profiles, with a study analyzing samples from 100 participants revealing that 85% exhibited distinct biochemical changes post-ingestion. The chromatography techniques used allowed for precise identification of metabolites linked to neurotransmitter receptor activity, influencing behavior in notable ways. This quantitative analysis highlights the potential of advanced sensing techniques in drug studies, establishing a clearer connection between chemical composition and psychological effects. Understanding these metabolites could pave the way for innovative approaches in biochemistry and mental health treatment.

Pharmacokinetics and subjective effects of 1P‐LSD in humans after oral and intravenous administration

Drug Testing and Analysis May 16, 2020 Christina Grumann, Kerstin Henkel, Simon D. Brandt et al. 23 citations

1P-LSD, a non-controlled alternative to LSD, acts as a prodrug that converts almost entirely into LSD in the human body. In two volunteers, oral and intravenous doses of 100 μg 1P-LSD were administered. After oral intake, only LSD was detected in serum and urine, with a terminal elimination half-life of about 6.4 hours. Intravenous 1P-LSD was detectable for only a few hours, while LSD persisted much longer. The bioavailability of LSD from oral 1P-LSD was nearly 100%. Subjective drug effects and altered states of consciousness scores were comparable to those from LSD, supporting the prodrug hypothesis. Oral administration produced higher 5D-ASC scores than intravenous.

Motivational structure of ayahuasca drinkers in social networks

Journal of Psychedelic Studies November 9, 2018 Tom Wolff, Torsten Passie 10 citations

Western ayahuasca drinkers who are active in online forums are typically 28–50 years old, hold higher education degrees, have prior experience with other psychedelic drugs and psychospiritual methods, and are motivated to drink ayahuasca again, usually in organized events like shamanic ceremonies or retreats. Their motivation is composed of four main elements: self-exploration, spiritual purposes, physical health issues, and sensation seeking. Self-exploration and spiritual purposes are the dominant reasons, while physical health and sensation seeking are minor. This motivational structure differs from that of local ayahuasca shaman clients in the upper Amazonas region.

Acute psychotropic, autonomic, and endocrine effects of 5,6-methylenedioxy-2-aminoindane (MDAI) compared with 3,4-methylenedioxymethamphetamine (MDMA) in human volunteers: A self-administration study.

Drug testing and analysis September 1, 2024 Verena Angerer, Yasmin Schmid, Florian Franz et al. 6 citations

In six healthy volunteers, the new psychoactive substance MDAI at 3.0 mg/kg produced subjective effects comparable to 125 mg of MDMA, including increased blood pressure, but did not raise heart rate or body temperature. MDAI increased cortisol and prolactin levels, appeared in serum about 20 minutes after ingestion, and remained detectable for at least 4 days in serum and 6 days in urine. The drug was well tolerated. Further research is needed to evaluate whether MDAI might have medicinal applications.

A model training curriculum for psychedelic, psycholytic, and entactogen-assisted psychotherapy.

Journal of psychopharmacology (Oxford, England) June 10, 2025 Torsten Passie, Anja Loizaga-Velder, Alicia Danforth et al. 4 citations

A consensus-based model curriculum for education and training in substance-assisted psychotherapy (SAP) covers theoretical topics and practical components including apprenticeship observation, ongoing clinical supervision, and self-experience for trainees. The model, developed by authors with extensive SAP experience, also addresses peer and conventional supervision, respect for intercultural differences, and teachings about indigenous use of related substances. It is largely adapted to western industrialized countries with established graduate-level psychotherapy training. The curriculum may be valuable for psychedelic researchers, those training therapists for research studies, and those preparing for clinical work outside research settings.

A history of the European Medical Society for Psycholytic Therapy (EPT) 1964–1974

Drug Science Policy and Law January 1, 2024 Torsten Passie 4 citations

The so-called psychedelic renaissance has revived interest in therapies using drugs like LSD and psilocybin. In 1960s and 1970s Europe, the dominant approach was psycholytic therapy, which used serial low-dose sessions embedded in long-term psychotherapy, grounded in psychoanalysis. Today, this method is largely neglected in favor of high-dose psychedelic peak therapy with minimal psychotherapy. The European Medical Society for Psycholytic Therapy (EPT), founded in 1965, coordinated LSD therapists, promoted professional exchange, and aimed to develop treatment and training standards, yet its history has been virtually undocumented. The author reconstructs the EPT's history from unique archival resources to inform future standards.

The History of MDMA

June 29, 2023 Torsten Passie 4 citations

MDMA's history is a mosaic of parallel developments across research, politics, recreational use, and medicine, not a simple linear story. The book traces MDMA from its early pharmaceutical origins after 1900, through its studied military potential and early psychotherapeutic use, to its spread as a recreational drug in Europe and the United States. Later chapters address debates over its toxicity, its global distribution as a dance drug since the 1990s, and recent research into its therapeutic potentials. The account integrates multiple narratives and levels of interaction to make this complex history more intelligible.

Early Use in Psychotherapy

The History of MDMA June 29, 2023 Torsten Passie 2 citations

From 1977, a small number of psychiatrists and psychotherapists used MDMA as an aid in psychotherapy, finding it suppressed the fear response and allowed patients to reprocess painful memories without the ego-disruption typical of other psychedelics. It was also applied in couple therapy, enabling communication free from anxiety-driven limitations. Therapists initially kept the substance secret, fearing it would share LSD's fate, but their research covered a few hundred patients with apparent success. The chapter recounts this early therapeutic history, describes five therapists and their work, and details the eventual scheduling of MDMA and the fate of FDA research protocols.

Hanscarl Leuner und die Grundlagen der Psycholytischen Therapie

Nervenheilkunde April 1, 2024 Torsten Passie 1 citation

Hanscarl Leuner (1919–1996) was the central figure of psycholytic therapy in Europe, which uses low doses of hallucinogens like LSD or psilocybin to loosen defense structures and access unconscious conflicts. Unlike psychedelic therapy, which relies on 1–2 high-dose sessions for mystical experiences, psycholytic therapy involves 5–25 substance applications embedded in long-term psychotherapy. The approach focuses on personal themes both during altered states and in regular sessions. This article outlines the fundamentals of psycholytic therapy and presents Leuner's research on its foundations.

The Scheduling

The History of MDMA June 29, 2023 Torsten Passie 1 citation

In 1984, the DEA proposed placing MDMA into Schedule I after learning of its broader distribution. Physicians using MDMA in therapy requested hearings, which were held in three U.S. cities before a DEA administrative law judge. The judge evaluated evidence on safety, medical use, abuse potential, and neurotoxicity, concluding MDMA should be Schedule III, not I. The DEA overruled its own judge and permanently placed MDMA into Schedule I in 1986. Before the hearings, the DEA had imposed emergency scheduling and successfully initiated international scheduling by the WHO, which nonetheless recommended allowing research on the substance.

The Toxicity Debate

The History of MDMA June 29, 2023 Torsten Passie 1 citation

The history of research on MDMA toxicity includes early deaths and neurotoxicity studies, often compromised by biased methodologies. A notable scandal involved a Johns Hopkins researcher who mistakenly administered methamphetamine instead of MDMA to monkeys, falsely linking MDMA to Parkinson's disease. Later studies on recreational users found mixed results, but a study of Mormon subjects who used only MDMA showed no long-term cognitive effects. The chapter also discusses how research results have been used in anti-Ecstasy campaigns.

MDMA as a Dance Drug

The History of MDMA June 29, 2023 Torsten Passie 1 citation

The connection between drugs and dancing has existed since ancient times, with parallels between medieval 'dance epidemics' and modern MDMA use at dance parties. MDMA's synergy with dancing spontaneously emerged around 1983 when enthusiast Michael Clegg sold it in Texas nightlife, leading to its rapid spread as a 'dance drug'. From 1985, MDMA reached Europe via Ibiza's dance scene, where UK disc jockeys became enthusiasts and launched MDMA-fueled parties in London. The Netherlands, with tolerant drug policies and Amsterdam's trade, became a distribution hub. The text outlines musical style evolution, key events, and ravers' positive and negative experiences.