Efficacy of vaginal cleansing in Cesarean Delivery

Efficacy of vaginal cleansing in reducing postoperative infection after Cesarean Delivery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240713062414N1

Enrollment

205

Registered

2024-08-03

Start date

2024-08-10

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

Condition 1: postoperative infection after Cesarean Delivery such as:endometritis. Condition 2: postoperative infection after Cesarean Delivery such as:wound infection. Infection of obstetric surgical wound

Interventions

Intervention 1: Control group: cesarean section will be performed routinely in these people. Intervention 2: Intervention group: in the intervention group of preoperative patients in addition routine

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: All woman with cesarean indications Obtaining informed consent to enter the study

Exclusion criteria

Exclusion criteria: Women with chorioamnionitis Allergy for povidon iodine Vaginal bleeding from placenta previa Active genital herpes

Design outcomes

Primary

Measure	Time frame
The percentage of people who have wound infection. Timepoint: Wound infection that will be checked one day,one week,and six weeks after surgery. Method of measurement: Physical examination and vaginal exam with speculum and thermometer.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSalameh Dadgar

Mashhad University of Medical Sciences

Dadgars@mums.ac.ir+98 51 3876 0126

Outcome results

None listed

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