CompletedN/ALSD

Salivary Oxytocin as a Biomarker in Psychedelic Assisted Psychotherapy

Sponsored by Tatiana Aboulafia Brakha

NCT ID
NCT06557239
Target Enrollment
10 participants
Start Date
2024-08-05
Est. Completion
2024-12-11

About This Study

The main objective of this pilot study is to obtain preliminary data on the reactivity of salivary oxytocin during a single LSD intake as part of PAP treatment for anxiety disorders or depression (treatment authorisations granted in advance by the Federal Officie of Public Health for compassionate use of the substance). There will be no interference with the usual clinical routine in our Service. The protocol is only for taking additional saliva measurements to measure oxytocin levels on the day of treatment. Participants will be asked to give 4 saliva samples the day of their LSD treatment .In addition they will fill-in self-report questionnaires which are part of the clinical routine

Conditions Studied

Depression, Anxiety

Interventions

  • Lysergic Acid Diethylamide (LSD)

Eligibility

Age:18 Years - 50 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* ongoing psychotherapy with a certified psychotherapist, anxiety disorder or depression resistant to usual treatments, agreement to stop necessary medication

Exclusion Criteria:

* Exclusion: psychotic or bipolar disorder, high suicidal risk, severe cardiovascular disease, severe liver disease, neurological disease of the central nervous system, pregnancy and breastfeeding

Study Locations (1)

Geneva University Hospitals
Geneva, Switzerland

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source

Salivary Oxytocin as a Biomarker in Psychedelic Assisted Psychotherapy | Huxley