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Study identifier: NCT06789705 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Plasma Oxytocin Changes in Response to Low-dose MDMA vs. Placebo in Patients With Arginine Vasopressin Deficiency and Healthy Controls

Condition: Central Diabetes Insipidus  ·  Sponsor: University Hospital, Basel, Switzerland

PhaseNA
Planned participants24
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The investigator hypothesize that low-dose MDMA (3,4-methylenedioxymethamphetamine) will produce a sufficiently strong oxytocin stimulation in healthy controls and no relevant increase in patients. This study will confirm previously published data and provide important safety data with low-dose MDMA stimulation testing.

This description comes directly from the study's public registry record.

Talk to the study team

Mirjam Christ-Crain, Prof.  ·  +41 61 265 25 25  ·  Mirjam.Christ-Crain@usb.ch

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital BaselBasel, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT06789705