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The effect of preoperative vaginal povidone Iodine preparation on post cesarean infection

The effect of preoperative vaginal povidone Iodine preparation on post cesarean infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138706201233N1
Enrollment
284
Registered
2009-02-09
Start date
2008-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Post-cesarean infection. Other puerperal infections

Interventions

Intervention 1: One gr parenteral cephazoline half an hour before operation. Intervention 2: vaginal scrub with povidone-Iodine solution plus 1 gr parenteral cephazoline half an hour before operation.
Prevention
One gr parenteral cephazoline half an hour before operation
vaginal scrub with povidone-Iodine solution plus 1 gr parenteral cephazoline half an hour before operation

Sponsors

Vice-chancellor for research department
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Being candidate for non emergent cesarean delivery. Exclusion criteria: history of sensitivity to betadine, chorio amnionitis, Active genital Herpes during pregnancy , any purulent discharge with pruritus or dysuria or malodor discharge during pregnancy, emergency cesarean section, fetal distress, vaginal bleeding due to placenta previa or placental abruption, no time for vaginal preparation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence of Fever. Timepoint: Before Cesarean section, and at the end of week 1 , 2, 3 , 4, 5, and 6 after operation. Method of measurement: Temperature>38 degree centigrade by oral thermometer.;Uterine fundal tenderness. Timepoint: Before intervention,one month and after intervention 6 monthes. Method of measurement: Uterine palpation (Physical examination).;Incidence of wound infection. Timepoint: Before intervention,one month and after intervention 6 monthes. Method of measurement: Purulent discharge, pruritus.

Secondary

MeasureTime frame
Incidence of endometritis. Timepoint: Before Cesarean section, and at the end of week 1 , 2, 3 , 4, 5, and 6 after operation. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Asgharnia

Guilan University of Medical Science, Rasht, Iran

Asgharnia@gums.ac.ir+98 13 1322 5624

Outcome results

None listed

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