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Clinical Analysis of Intraperitoneal Cesarean Section Versus Extraperitoneal Cesarean Section Under the Concept of Enhanced Recovery

Clinical Analysis of Intraperitoneal Cesarean Section Versus Extraperitoneal Cesarean Section Under the Concept of Enhanced Recovery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124812
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-20
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Intraperitoneal and Extraperitoneal Cesarean Section

Interventions

Group 1:Intraperitoneal cesarean section + CSEA + postoperative transversus abdominis plane block
Group 2:Intraperitoneal cesarean section + CSEA + postoperative transversus abdominis plane block
Group 3:Intraperitoneal cesarean section + CSEA (control group)

Sponsors

The First Hospital of Handan City, Hebei Province
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed singleton pregnancy; 2. Have carefully read the informed consent form and voluntarily agree to participate; 3. Age: 18–35 years; 4. Gestational weeks: 37–42 weeks; 5. No history of severe psychiatric disorders; 6. No history of depression, anxiety, or other related disorders; 7. No severe dysfunction of vital organs such as heart, liver, or kidneys.

Exclusion criteria

Exclusion criteria: 1. Pathological obstetric conditions such as placenta previa, placental abruption, moderate preeclampsia, or need for general anesthesia; 2. Patients with ovarian malignancy during pregnancy, pregnancy with uterine malformation, threatened uterine rupture, or uterine rupture requiring emergency cesarean section; 3. Cognitive impairment, mental disorders, or inability to communicate effectively; 4. Pre-existing severe infection (e.g., sepsis) before surgery; 5. Pregnancy complicated by obesity (BMI >=30); 6. Estimated fetal weight > 4000 g.

Design outcomes

Primary

MeasureTime frame
postoperative time to first passage of flatus.;Visual Analogue Scale score at rest and on activity;

Secondary

MeasureTime frame
Time to first ambulation (hours);Length of hospital stay;Time to first analgesic request;Self-Rating Anxiety Scale (SAS) score;Edinburgh Postnatal Depression Scale (EPDS) score;Operative time (minutes);Intraoperative blood loss;Total inpatient cost;

Countries

China

Contacts

Public ContactXue Jie

The First Hospital of Handan City

xuejie1980@126.com+86 158 3300 8300

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026