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Effect of povidone-iodine and chlorhexidine on prevention of infection after emergency cesarean section

Comparison of the effectiveness of vaginal cleansing with povidone-iodine versus chlorhexidine before emergency cesarean section in preventing surgical site infections: a double-blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250329065173N1
Enrollment
170
Registered
2025-10-06
Start date
2025-10-23
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Surgical site infections following emergency cesarean section.

Interventions

Intervention 1: Intervention group: Vaginal douching to chlorhexidine solution
Intervention: Vaginal wash with 0.5% chlorhexidine solution before emergency cesarean section
Dose and amount: 10 mL of 0.5% chlorhexidine solution
Frequency: Once, 30 minutes before the surgical procedure
Duration: Single session prior to surgery
Method of administration: Chlorhexidine solution is instilled into the vagina using a sterile syringe and drained after 5 minutes
Equipment and materials: 10 mL sterile syringe, 0.5% chlorhexidine solution, sterile gloves
Manufacturer: Tehran Shimi Pharmaceutical Company. Intervention 2: Control group: Intervention: Vaginal wash with 10% povidone-iodine solution (Betadine) before emergency cesarean section
Dose and amount: 10 mL of 10% povidone-iodine solution
Method of administration: Povidone-iodine solution is instilled into the vagina using a sterile syringe and drained after 5 minutes
Equipment and materials: 10 mL sterile syringe, 10% povidone-iodine solution, sterile gloves
Manufacturer: Tehran Shimi Pharmaceutical Company.

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Gestational age between 37 and 42 weeks (term pregnancy) Singleton pregnancy Maternal age = 18 years Need for emergency cesarean section General condition suitable for tolerating the intervention and follow-up

Exclusion criteria

Exclusion criteria: Patients with allergy to povidone-iodine or chlorhexidine Patients with signs of chorioamnionitis or fever during labor, or other signs of infection Active vaginal or genital infection at the time of surgery History of previous infections related to wound or vagina Unstable underlying disease Lack of willingness or ability to sign the informed consent form Inability to follow up after surgery Presence of chorioamnionitis or fever before cesarean section

Design outcomes

Primary

MeasureTime frame
Fever = 38°C. Timepoint: Days 1, 7, 15, and 30 after cesarean section. Method of measurement: Body temperature measured with a digital thermometer by a trained nurse.;Wound redness. Timepoint: Days 1, 7, 15, and 30 after cesarean section. Method of measurement: Clinical examination by a trained nurse.;Wound swelling. Timepoint: Days 1, 7, 15, and 30 after cesarean section. Method of measurement: Clinical examination by a trained nurse.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Fazel

Sabzevar University of Medical Sciences

shohreh1368@yahoo.co.uk+98 51 4401 8301

Outcome results

None listed

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