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Effects of esketamine combined with dexmedetomidine on depression and pain in pregnant women with sleep disorders after cesarean section

Effect of esketamine combined with dexmedetomidine on postpartum depression and pain in women who delivered cesarean section with sleep disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099016
Enrollment
Unknown
Registered
2025-03-17
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Postpartum depression

Interventions

Control group:After delivery, 0.5ug/kg dexmedetomidine was injected intravenously for 10min, followed by PCIA pump: dexmedetomidine 100ug+ sufentanil 50ug+ normal saline, total 100ml, continuous flow
Experimental group:After delivery, 0.5ug/kg of dexmedetomidine and 0.3mg/kg of esketamine were injected intravenally for 10min, followed by PCIA pump: 100ug of dexmedetomidine + 50mg of esketamine + n

Sponsors

Wenzhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Women with cesarean section under neuraxial anesthesia; 2. > = 18 years old; 3. ASA Level II; 4. > gestation = 28 weeks; 5. Require postoperative intravenous self-controlled analgesia; 6. Preoperative Pittsburgh Sleep Quality Index (PSQI) >=7 points; 7. The mother can communicate well with the follow-up patients, understand the trial process and voluntarily participate in the study and sign the relevant informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of mental illness or depression in the past; 2. Severe cardiovascular and cerebrovascular diseases and liver and kidney insufficiency; 3. Have a history of psychotropic drugs and alcohol abuse; 4. Severe eclampsia; 5. Allergy to the drugs in this trial; 6. Placenta previa, placental abruption and other diseases with estimated blood loss greater than 800 ml before surgery; 7. Preoperative sinus bradycardia (maternal heart rate less than 50 beats/min), or abnormal heart conduction or heart rhythm diseases such as sick sinus syndrome; 8. Preoperative hypotension (standard systolic blood pressure less than 90mmHg and/or diastolic blood pressure less than 60mmHg); 9. Unable to understand the language of the follow-up and communicate well.

Design outcomes

Primary

MeasureTime frame
EPSD scores ;

Secondary

MeasureTime frame
Incidence of self-harm ideation;LSEQ score;VAS score;Remedial analgesic situation;Surgical and anesthesia-related indicators;Postoperative conditions and adverse reactions;

Countries

China

Contacts

Public ContactJing Chen

Wenzhou People's Hospital

765391718@qq.com+86 137 3877 6614

Outcome results

None listed

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