Clinical Trials Directory

Trials / Completed

CompletedNCT03927378

Low-dose S-Ketamine and Postpartum Depression in Parturients With Prenatal Depression

Effects of Low-dose S-Ketamine on Incidence of Postpartum Depression in Parturients With Prenatal Depression: A Randomized, Double-blind, Placebo-controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
364 (actual)
Sponsor
Peking University First Hospital · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Prenatal depression is an important risk factor of postpartum depression. Low-dose ketamine has been used for depression treatment. As a stereoisomer of ketamine, s-ketamine has similar effects to ketamine in anti-depression. We speculate that, for pregnant women with prenatal depression, low-dose s-ketamine infusion after childbirth may reduce the incidence of postpartum depression.

Detailed description

Studies have shown that prenatal depression symptoms are important predictors of postpartum depression. Screening of pregnant women's mental condition before giving birth, early identification of pregnant women with symptoms of prenatal depression, and providing appropriate interventions may play an important role in reducing the incidence of postpartum depression. Ketamine is an NMDA-receptor antagonist. In recent years, many studies confirmed that ketamine has a significant antidepressant effect. As a stereoisomer of ketamine, s-ketamine has similar effects to ketamine in anti-depression. In clinical application, s-ketamine has stronger analgesic effect, better anesthetic effect and lower incidence of adverse psychological reactions. We speculate that, for pregnant women with prenatal depression, low-dose s-ketamine infusions after childbirth may reduce postpartum depression. Evidence is lacking in this regard.

Conditions

Interventions

TypeNameDescription
DRUGS-ketamineS-ketamine (0.2 mg/kg in 20 ml normal saline) is administered by intravenous infusion in 40 minutes after childbirth.
DRUGPlaceboPlacebo (20 ml normal saline) is administered by intravenous infusion in 40 minutes after childbirth.

Timeline

Start date
2020-06-19
Primary completion
2022-08-03
Completion
2022-08-03
First posted
2019-04-25
Last updated
2023-04-04

Locations

7 sites across 1 country: China

Source: ClinicalTrials.gov record NCT03927378. Inclusion in this directory is not an endorsement.