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Effect of low-dose esketamine on pain control and postpartum depression after cesarean section: A double-blind randomized controlled trial

Effect of low-dose esketamine on pain control and postpartum depression after cesarean section: A randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200067054
Enrollment
Unknown
Registered
2022-12-26
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Postoperative acute pain and Depressed

Interventions

Control goup:PCIA(Sufentanil 100ug+Palonosetron0.5mg+0.9% normal saline to 100ml)
Intervention group:PCIA((Esketamine 1mg ? kg-1+sufentanil 100ug+Palonosetron 0.5mg+normal saline to 100ml))

Sponsors

Fisrt Hospital of Putian, Putian,Fujian
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) The elective operation conforms to the indication of cesarean section; (2) No contraindication of spinal anesthesia. (3) American Association of Anesthesiologists (ASA) Grade I - II.

Exclusion criteria

Exclusion criteria: (1) Pathological obstetric diseases; (2) People with depression and other mental symptoms; (3) People with drug allergy; (4) History of alcohol or drug dependence for more than 6 months; (5) History of ketamine abuse or dependence; (6) Those with abnormal coagulation function, liver and kidney function, or hypertension or diabetes; (7) Poor compliance, midway spontaneous labor to cesarean section.

Design outcomes

Primary

MeasureTime frame
Visual analog scale score;

Secondary

MeasureTime frame
free cortisol;atrial natriureticpeptide;epinephrine;Nepinephrine;Cognitive dysfunction;edinburgh postpartum depression scale;

Countries

China

Contacts

Public ContactShurong Li

Fisrt Hospital of Putian, Putian,Fujian

lsrywpt@163.com13959579688

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026