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Effects of different administration methods of esketamine on the prevention of postpartum depression : a randomized controlled trial

Effects of different administration methods of esketamine on the prevention of postpartum depression : a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082919
Enrollment
Unknown
Registered
2024-04-11
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum depression, PPD

Interventions

Blank control group ( group C ):None
Esketamine injection group ( group I ):After umbilical cord clamping in cesarean section, a single intravenous injection of esketamine 0.25 mg / kg ( diluted with normal saline to 20 ml, intravenous i
Esketamine pump injection group ( group P ):After umbilical cord clamping in cesarean section, a continuous intravenous infusion of esketamine 0.25 mg / kg ( diluted with normal saline to 20 ml, intra

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Full-term singleton puerpera were scheduled for elective cesarean section under intraspinal anesthesia. 2. ASA?~?. 3. Aged from 20 to 45 years. 4. BMI 18~30 kg/m2. 5. Edinburgh Postpartum Depression Scale score < 10 points before cesarean section.

Exclusion criteria

Exclusion criteria: 1. Contraindications for the use of esketamine. 2. Application of sedative hypnotics and antidepressants within a week. 3. With a history of drug abuse. 4. Allergic to local anesthetics. 5. With severe heart, lung, liver and kidney dysfunction.

Design outcomes

Primary

MeasureTime frame
The incidence of PPD at 6 weeks after operation ( PPD was defined as Edinburgh Postnatal Depression Scale ( EPDS ) score = 10 points at 6 weeks after operation ).;

Secondary

MeasureTime frame
EPDS score at 3 days, 1 week, 4 weeks and 6 weeks after operation.; Pain VAS score and Brief Psychiatric Rating Scale ( BPRS + ) score at 1 day, 2 days and 3 days after operation.;

Countries

China

Contacts

Public ContactRen Li

The First Affiliated Hospital of Chongqing Medical University

renli177@163.com+86 183 2318 7421

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026