Treatment of Chorioamnionitis After Delivery
Chorioamnionitis
About this trial
This is an interventional treatment trial for Chorioamnionitis focused on measuring chorioamnionitis, antibiotics, cesarean, vaginal delivery
Eligibility Criteria
Inclusion Criteria:.
- All patients that develop chorioamnionitis and who are over 18 years of age will be offered participation in the study.
Exclusion Criteria:
- Women who do not wish to participate, patients who are allergic to the study antibiotics
- Women who are immunocompromised or women receiving antibiotics for other reasons such as prophylaxis for bacterial endocarditis
Sites / Locations
- Naval Medical Center - PortsmouthRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Active Comparator
Other
Other
vaginal delivery 1
vaginal delivery antibotics2
cesarean delivery one dose3
cesarean multiple antibiotics 4
no further antibiotics after delivery (the patient will receive a saline infusion instead of antibiotics)
one additional dose of antibiotics (ampicillin 2 grams IV, gentamicin 1.5 mg/kg IV) following vaginal delivery
one dose of ampicillin 2 grams IV, gentamicin 1.5 mg/kg IV, clindamycin 900 mg IV and then saline infusions instead of antibiotics until they are afebrile for 24 hours ( they will receive saline infusions instead of antibiotics)
ampicillin 2 g IV every 6 hours, gentamicin 1.5mg/kg every 8 hours, and clindamycin 900 mg IV every 8 hours until the patient has been afebrile for 24 hours