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Clinical Trial Summary

To evaluate the rate of infections after cesarean sections in patients with premature rupture of membranes after vaginal wash either with an antiseptic solution (clorhexidine solution) vs. saline solution (placebo).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03442218
Study type Interventional
Source Saint Thomas Hospital, Panama
Contact
Status Completed
Phase N/A
Start date June 1, 2017
Completion date February 28, 2018

See also
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