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
| Type | Name | Description |
|---|---|---|
| DRUG | S-ketamine | S-ketamine (0.2 mg/kg in 20 ml normal saline) is administered by intravenous infusion in 40 minutes after childbirth. |
| DRUG | Placebo | Placebo (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.