Use of Postpartum uterine curettage in reducing hospitalization time or in improving the
clinical evolution of the patient with preeclampsia/eclampsia.
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Full eligibility criteria for NCT03028194
Ages eligible for Study
15 Years to 40 Years
Genders eligible for Study
Accepts Healthy Volunteers
Gestational age 24 weeks or more.
Epilepsy or seizures previous to pregnancy.
All locations for NCT03028194
Saint Thomas H
Saint Thomas Maternity Hospital
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Tris trial is registered with FDA with number: NCT03028194. The sponsor of the trial is Saint Thomas Hospital, Panama and it is looking for 442 volunteers for the current phase.
Official trial title: Effects of Postpartum Uterine Curettage in the Recovery From Preeclampsia/Eclampsia: A Randomized, Controlled Trial
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