Geneva, March 23 -- International Clinical Trials Registry received information related to the study (ChiCTR2600119684) titled 'Clinical Study on Postoperative Infection Following Intrapartum or Post-Rupture of Membranes Cesarean Section' on March 2.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Peking University Third Hospital
Condition:
Obstetric Infection
Intervention:
Control group:None
Povidone-Iodine Vaginal Disinfection Group:For preoperative preparation for cesarean section, disinfect the vagina using povidone-iodine.
Recruitment Status: Recruiting
Phase: N/A
Date of First Enrollment: 2026-02-09
Target Sample Size: Control group:300;Povidone-Iodine Vaginal Disinfection Group:300;Chlorhexid...