WHO ICTRP trial
Clinical Study on the Effects of Low-dose Esketamine via Single Intravenous…
ChiCTR2500115402 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR2500115402 |
|---|---|
| Public title | Clinical Study on the Effects of Low-dose Esketamine via Single Intravenous Injection on Postpartum Depression in Parturients Undergoing Labor Analgesia |
| Scientific title | Clinical Study on the Effects of Low-dose Esketamine via Single Intravenous Injection on Postpartum Depression in Parturients Undergoing Labor Analgesia |
| Primary sponsor | Affiliated hangzhou first people's hospital, zhejiang university school of medicine |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Countries | China |
| Conditions | Full-term singleton primiparous women undergoing vaginal delivery |
| Interventions | Control group (Normal saline group):Placebo (normal saline);Trial group (Esketamine group):Intravenous administration of esketamine (0.2 mg/kg) after fetal delivery. |
| Registration date | Dec 25, 2025 |
| Target size | Control group (Normal saline group):55;Trial group (Esketamine group):55 |
| Registry page | chictr.org.cn |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: