NCT03028194View on ClinicalTrials.gov

Postpartum Uterine Curettage in the Recovery From Preeclampsia/Eclampsia

NACompletedINTERVENTIONAL
Enrollment

442

Participants

Timeline

Start Date

October 1, 2015

Primary Completion Date

October 31, 2016

Study Completion Date

December 11, 2016

Conditions
Pre-EclampsiaEclampsia
Interventions
PROCEDURE

Curettage

Postpartum uterine curettage with a sharp curette # 14 or #16, immediately after delivery of the placenta.

PROCEDURE

Placebo

No procedure after delivery of the placenta

Trial Locations (2)

Unknown

Saint Thomas H, Panama City

Saint Thomas Maternity Hospital, Panama City

All Listed Sponsors
lead

Saint Thomas Hospital, Panama

OTHER

NCT03028194 - Postpartum Uterine Curettage in the Recovery From Preeclampsia/Eclampsia | Biotech Hunter | Biotech Hunter