drugset / Trial / NCT04227704

Ketamine to Prevent PPD After Cesarean

NCT04227704

Phase 3 Completed 25 enrolled Washington University School of Medicine
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The investigators plan to randomise participants to receive ketamine or placebo control subcutaneously or by 40-minute intravenous infusions and will follow them up for 42 days to assess the incidence of postpartum depression. This feasibility pilot study is designed to explore the adequacy of the study procedures and tolerability of the interventions.

Timeline

Start
2020-11-12
Primary completion
2021-08-09
Completion
2021-08-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketamine Small molecule 0.5 mg/kg Subcutaneous

Indications