drugset / Trial / NCT04227704
Ketamine to Prevent PPD After Cesarean
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ketamine | Small molecule | 0.5 mg/kg | Subcutaneous |