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Preoperative sleep disturbance exacerbates postoperative pain after cesarean delivery: A prospective clinical cohort study

Preoperative sleep disturbance exacerbates postoperative pain after cesarean delivery: A prospective clinical cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109909
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Postoperative acute pain

Interventions

No sleep deficiency group(NSD group):None

Sponsors

Jinan Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Term pregnancy 2. Singleton gestation 3. No contraindications to combined spinal-epidural (CSE) anesthesia, including coagulopathy, anticoagulant therapy, severe hypovolemia, or hemodynamic instability 4. Planned cesarean delivery

Exclusion criteria

Exclusion criteria: 1. History of psychiatric disorders, central nervous system diseases, liver disease, renal dysfunction, or cardiopulmonary abnormalities 2. Severe obstetric complications, such as placenta previa or placental abruption 3. BMI > 35 4. No participation in any other clinical study within the past 6 months 5. Patient refusal to participate

Design outcomes

Primary

MeasureTime frame
pain score AUC within 24 hours postoperatively.;

Secondary

MeasureTime frame
the usage rate of indomethacin suppositories;chronic pain;the number of presses on the analgesic pump;postpartum depression;Pain score postoperatively.;Postoperative complications;

Countries

China

Contacts

Public ContactMeng Fanqing

Jinan Maternal and Child Health Care Hospital

mengfanqing8211@126.com+86 531 89029618

Outcome results

None listed

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