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Clinical trial

Ketamine to Prevent PPD After Cesarean

Washington University School of MedicineCompletedPhase 3Started Nov 12, 202025 enrolledUnited StatesNCT04227704

Abstract

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.

Topics & conditions

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KetamineDepression

Keywords

Postpartum Depression

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