drugset / Trial / NCT05128071

PRevention Of Methamphetamine Use Among Postpartum Women Trial (PROMPT)

NCT05128071

Phase 0 Completed 34 enrolled University of Utah
RandomizedParallel-groupTriple-blindTreatment

Summary

The PRevention Of Methamphetamine Use among Postpartum Women Trial (PROMPT) is randomized controlled trial of postpartum individuals with methamphetamine use disorder to 12 weeks of 200 mg oral micronized progesterone twice daily or placebo. The aims of this study are to assess the feasibility, safety and preliminary efficacy of micronized progesterone for the prevention of return to methamphetamine use. A secondary aim is to assess participant's salivary levels of allopregnanolone with methamphetamine cravings. This study has the potential to provide effective interventions to prevent methamphetamine use among postpartum women.

Timeline

Start
2022-02-04
Primary completion
2024-05-30
Completion
2024-05-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Progesterone Other / unclassified 200 mg Oral