Clinical TrialID 7976
Acute Effects of 3,4-methylenedioxymethamphetamine (MDMA) With and Without a Booster Dose
NCT05809271
Healthy
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 7976
- Evidence Id
- 7976
- Core Evidence Id
- 7976
- Source Clinical Trial Id
- 7971
- Herb2 Clinical Trial Id
- HBCT007971
- Nct Id
- NCT05809271
- Title
- Acute Effects of 3,4-methylenedioxymethamphetamine (MDMA) With and Without a Booster Dose
- Status
- Recruiting
- Phase
- Phase 1
- Study Result
- No
- Study Condition
- Healthy
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: TRIPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR)|Primary Purpose: BASIC_SCIENCE
- Intervention
- DRUG: MDMA 120 mg + MDMA 60 mg|DRUG: MDMA 120 mg + placebo|DRUG: Placebo
- Intervention Allocation
- Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Triple
- Intervention Purpose
- Basic_Science
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 24
- Outcome Measure
- Subjective effect duration for "any drug effect", Assessed by visual analog scale (VAS) using 10% of the individual maximal subjective response (Emax) as threshold for the onset and offset., Every 15 minutes for 9 hours after substance administration
- Sponsor Collaborator
- University Hospital, Basel, Switzerland
- Funded By
- OTHER
- Location
- University Hospital, Basel, 4031, Switzerland
- Other Id
- BASEC 2023-00167
- Start Date
- 2023-11-17
- Primary Completion Date
- 2025-12-31
- Completion Date
- 2025-12-31
- First Posted
- 2023-04-12
- Results First Posted
- Last Update Posted
- 2023-11-21
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05809271
- Title Cn
- Title En
- Acute Effects of 3,4-methylenedioxymethamphetamine (MDMA) With and Without a Booster Dose
- Bilingual Status
- semi_complete