Evaluation of intrauterine balloon tamponade efficacy with condom catheter in the severe postpartum hemorrhage management in Benin and Mali

Not Applicable

Completed

• Conditions: Gynecology-obstetrical/severe postpartum hemorrhage; Pregnancy and Childbirth; Postpartum haemorrhage

• Registration Number: ISRCTN01202389
• Lead Sponsor: Institute of Research for Development (Institut de Recherche pour le Développement) (IRD)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-09-09
• Last Update Posted: 13 March 2017

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

1. Having given birth by vaginal way, in one of the selected establishments
2. After 28 weeks of amenorrhea, or foetus > 1000 g
3. Presenting a HPPI resisting the oxytocine and the first-line laborers (uterine massage + uterine revision)
4. Having given its oral consent

Exclusion Criteria

1. Having given birth by caesarian
2. Presenting a contraindication or an allergy known about prostaglandins
3. Presenting an allergy to latex
4. Presenting a clinical Chorioamnionitis
5. Presenting a secondary postpartum hemorrhage, cervico-vaginal tears without uterine bleeding, an uterine break, or a placenta accreta

Study & Design

• Study Type: Interventional
• Study Design: Not specified