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Preoperative sleep deficiency affects postoperative pain after cesarean delivery: a prospective clinical cohort study

Preoperative sleep deficiency affects postoperative pain after cesarean delivery: a prospective clinical cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096601
Enrollment
Unknown
Registered
2025-01-26
Start date
2024-01-08
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Postoperative pain

Interventions

Sponsors

Jinan Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Full term pregnancy; 2.Singleton; 3.proposed for cesarean section; 4.no contraindications for combined spinal-epidural anesthesia, including abnormal coagulation function, anticoagulant therapy, severe hypovolemia or hemodynamic instability.

Exclusion criteria

Exclusion criteria: 1.Previous mental illness, central nervous system disease, liver disease, renal dysfunction, and cardiopulmonary dysfunction; 2.Severe obstetric complications, such as placenta previa or placental abruption; 3.Have participated in other clinical studies in the past 6 months; 4.The patient refuses to participate; 5.BMI>35.

Design outcomes

Primary

MeasureTime frame
Pittsburghsleep quality index, PSQI;Visual Analogue Scale,VAS;Area under the pain score curve;

Secondary

MeasureTime frame
Postoperative complication rate;

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