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A randomized controlled clinical study on early recovery after cesarean section

A randomized controlled clinical study on early recovery after cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091208
Enrollment
Unknown
Registered
2024-10-23
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

After cesarean section

Interventions

Rapid Rehabilitation Group:Rapid recovery management measures
Traditional Management Group:Traditional management measures

Sponsors

Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Voluntarily serving as a subject and signing an informed consent form; (2) Termination of pregnancy through elective cesarean section; (3) Full term pregnancy;

Exclusion criteria

Exclusion criteria: (1) Pernicious placenta previa hemorrhage; (2) Hemolytic liver dysfunction with thrombocytopenia (HELLP) syndrome; (3) Severe preeclampsia; (4) Severe heart disease; (5) Acute fatty liver during pregnancy; (6) Emergency cesarean section; (7) Coagulation dysfunction; (8) Pregnancy complicated with severe thrombocytopenia; (9) Pregnancy complicated with serious internal and external diseases; (10) Contraindications for spinal anesthesia; (11) Simultaneously participating in other clinical studies during the research period; (12) Suffering from contraindications for drug use; (13) History of anesthesia and related drug allergies; (14) Other situations assessed by the researchers as unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
First anal exhaust time after surgery;Length of hospital stay;

Secondary

MeasureTime frame
Postoperative pain score;Postoperative breastfeeding time;Postoperative breast milk volume;Postoperative physical recovery status;Postoperative uterine recovery status;Postoperative activity level;Hospitalization expenses;Satisfaction with hospitalization;Postoperative complications;Readmission status 42 days after surgery;

Countries

China

Contacts

Public ContactPing Li

Xiangya Hospital of Central South University

pingli11102@csu.edu.cn+86 186 8470 1850

Outcome results

None listed

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