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Postpartum Uterine Curettage in the Recovery From Preeclampsia/Eclampsia

NCT03028194 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 442

Last updated 2017-01-23

No results posted yet for this study

Summary

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

Conditions

  • Pre-Eclampsia
  • Eclampsia

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

Sponsors & Collaborators

  • Saint Thomas Hospital, Panama

    lead OTHER

Principal Investigators

  • Osvaldo Reyes, MD · Saint Thomas Hospital, Panama

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
15 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-01
Primary Completion
2016-10-31
Completion
2016-12-11

Countries

  • Panama

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03028194 on ClinicalTrials.gov