Postpartum Uterine Curettage in the Recovery From Preeclampsia/Eclampsia

Status Completed

Clinical Trial Summary

Use of Postpartum uterine curettage in reducing hospitalization time or in improving the clinical evolution of the patient with preeclampsia/eclampsia.

Clinical Trial Description

To evaluate if postpartum uterine curettage improved the clinical and laboratory parameters in patients with preeclampsia or eclampsia.

A total of 442 patients with preeclampsia/eclampsia were randomized to postpartum curettage (223) or no procedure (219). Systolic and diastolic blood pressure were recorded and analyzed at hours 6, 12, 24 and 48. Also, several laboratory values and diuresis were evaluated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03028194
Study type	Interventional
Source	Saint Thomas Hospital, Panama
Contact
Status	Completed
Phase	N/A
Start date	October 1, 2015
Completion date	December 11, 2016

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