drugset / Trial / NCT07189299

Microdosing LSD in Women With Premenstrual Disorders

NCT07189299 ↗

Not yet recruiting 150 enrolled Friederike Holze
RandomizedParallel-groupQuadruple-blindOther

Summary

The investigators aim to investigate the role of the serotonin 2A receptor in women with premenstrual disorders. This study uses a double-blind, randomized, controlled design with 3 arms: Intervention 1: 10 micg LSD for \~10 days during the late luteal phase (for 3 cycles) Intervention 2: 10 micg LSD every other day for \~10 days during the late luteal phase (for 3 cycles) Control intervention: Placebo for \~10 days during the late luteal phase (for 3 cycles) Each participant will be treated in only one arm. The study employs a parallel design with three treatment arms and consists of a two-cycle observational phase followed by a three-cycle treatment phase.

Timeline

Start
2025-10-01
Primary completion
2029-11-01
Completion
2030-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject LSD Unknown 10 ug —