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The effect of es-ketamine used in PCIA on postpartum depression after cesarean

The effect of es-ketamine used in PCIA on postpartum depression after cesarean

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050263
Enrollment
Unknown
Registered
2021-08-24
Start date
2019-09-01
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Postpartum Depression

Interventions

es-ketamine group:es-ketamine 0.5mg/kg used in patient controlled intravenous analgesia
control group:normoal PCIA used after cesarean but no es-ketamine

Sponsors

Henan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form; 2. No previous history of depression and brain diseases; 3. Full-term and singleton pregnant women undergoing cesarean section under selective subarachnoid anesthesia; 4. ASA classification I, II; 5. BMI 18~30 kg/m2

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to sign informed consent; 2. Those who have contraindications to subarachnoid anesthesia; 3. Patients with intractable, refractory hypertension or severe cardiovascular disease; 4. Patients with previous history of depression, and patients who have received or have not received antidepressant treatment; 5. Severe pathological obstetric conditions (pregnancy hypertension syndrome, eclampsia, placenta previa, placental abruption, etc.); 6. Those who are known to be allergic to the drugs used during surgery.

Design outcomes

Primary

MeasureTime frame
incidence of postpartum depression;

Secondary

MeasureTime frame
Edinburgh Postnatal Depression Scale (EPDS);Ramssy Sedation Scale Score;Visual Analogue Scale (VAS);incidence of side reacton;

Countries

China

Contacts

Public ContactJiaqiang Zhang

He'nan Provincial People's Hospital

hnmzxh@163.com+86 13937121360

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026