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

Not Applicable
Conditions
Post-cesarean infection.
Other puerperal infections
Registration Number
IRCT138706201233N1
Lead Sponsor
Vice-chancellor for research department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
284
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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.
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