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Bakri Balloon in Placenta Previa

Not Applicable
Withdrawn
Conditions
Bleeding
Placenta Previa
Interventions
Procedure: Abdominal traction stitch
Device: Bakri Balloon
Registration Number
NCT02694341
Lead Sponsor
Assiut University
Brief Summary

The Bakri intrauterine balloon can achieve haemostasis in cases of postpartum haemorrhage, including haemorrhage associated with placenta previa by compressing the lower uterine segment.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria
  1. All women delivered and presented with primary atonic PPH
  2. Women who accepted to participate
Exclusion Criteria
  1. Traumatic PPH as excluded by examination under anesthesia.
  2. With any suspected or clinical evidence of uterine infection
  3. Women diagnosed to have preeclampsia or eclampsia after delivery.
  4. Women who had DM during pregnancy
  5. Women with history of DVT or other thromboembolic complication
  6. Women with history of rheumatic heart disease.
  7. Women with coagulation defects.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Bakri Balloon with abdominal traction stitchBakri Balloonbakri balloon will be inserted with abdominal traction stitch
Bakri Balloon without abdominal traction stitchBakri Balloonbakri balloon will be inserted with no performance of abdominal traction stitch
Bakri Balloon with abdominal traction stitchAbdominal traction stitchbakri balloon will be inserted with abdominal traction stitch
Primary Outcome Measures
NameTimeMethod
Percentages of failure of Bakri Balloon either rupture of balloon or slippage of balloon.24 hours
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ahmed Abbas

🇪🇬

Assiut, Cairo, Egypt

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