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Effectivity of Postpartum Dexamethasone for Women With Class I HELLP Syndrome — COHELLP  

HELLP Syndrome Clinical Trial

Official title:
Postpartum Dexamethasone for Women With Class I HELLP Syndrome: a Double-blind, Placebo-controled, Randomized Clinical Trial

Clinical Trial Summary

Corticotherapy accelerates maternal postpartum recovery in women with class I HELLP syndrome. The benefit of faster and better recovery would be observed in fewer complications, less utilization of blood products and shorter hospital stay.

Clinical Trial Description

Patients with Class I HELLP Syndrome will be recruited for use os dexamethasone or placebo in the puerperium. Effects such as clinical course (blood pressure and diureses), laboratorial behaviour and complications will be compared. Duration of hospitalization will also be accessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00711841
Study type Interventional
Source Instituto Materno Infantil Prof. Fernando Figueira
Contact
Status Terminated
Phase Phase 4
Start date July 2011
Completion date June 2019
View Details
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