Antibiotic Prophylaxis in Prelabor Rupture of Membranes at Term

Status Completed

Clinical Trial Summary

The aims of this study are to determine whether antibiotics administered routinely in women presenting with premature rupture of membranes later than the 37+0 weeks of gestation can alter the rate of maternal and neonatal infection and to compare these rates between prompt (< 12 hour) and delayed (≥ 12 hour) induction in the group of patients not submitted to antibiotic prophylaxis.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01633294
Study type	Interventional
Source	Hospital de Santa Maria, Portugal
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	October 2008
Completion date	January 2012

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