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The present study was a prospective randomized controlled trial in which subjects received a vaginal preparation with povidone-iodine solution immediately prior to caesarean delivery or received no vaginal preparation
Full description
The present study was a prospective randomized controlled trial in which subjects received a vaginal preparation with povidone-iodine solution immediately prior to caesarean delivery or received no vaginal preparation
Enrollment
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Inclusion criteria
Exclusion criteria
• Betadine allegy.
Primary purpose
Allocation
Interventional model
Masking
1,200 participants in 2 patient groups
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Central trial contact
Heba Wagih, MD; Ahmed maged, MD
Data sourced from clinicaltrials.gov
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