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Clinical Study on Postoperative Infection Following Intrapartum or Post-Rupture of Membranes Cesarean Section

Clinical Study on Postoperative Infection Following Intrapartum or Post-Rupture of Membranes Cesarean Section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119684
Enrollment
Unknown
Registered
2026-03-02
Start date
2026-02-09
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Obstetric Infection

Interventions

Control group:None
Povidone-Iodine Vaginal Disinfection Group:For preoperative preparation for cesarean section, disinfect the vagina using povidone-iodine.
Chlorhexidine Acetate Vaginal Disinfection Group:For preoperative preparation for cesarean section, disinfect the vagina using Chlorhexidine Acetate.

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A total of 900 pregnant women who were hospitalized for delivery at Peking University Third Hospital and required cesarean section for termination of pregnancy after the onset of labor or rupture of fetal membranes.

Exclusion criteria

Exclusion criteria: Suspected allergy to disinfectants (iodophor or chlorhexidine acetate); Failure to obtain informed consent.

Design outcomes

Primary

MeasureTime frame
Surgical Site Infection;Postoperative Fever;Endometritis;Wound Complications;Neonatal Sepsis ;Pathological Chorioamnionitis ;—

Countries

China

Contacts

Public ContactLi Luyao

Peking University Third Hospital

63451416@qq.com+86 152 0128 5823

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026