Effectiveness of Balloon Tamponade with a Condom Catheter versus Using a Sengstaken-Blakemore Tube in Patients with Primary Postpartum Hemorrhage
Not Applicable
- Conditions
- Primary postpartum hemorrhage.
- Registration Number
- IRCT20221231056999N3
- Lead Sponsor
- Bahawal Victoria Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 64
Inclusion Criteria
Females aged between 18-40 years
Parity 1-6
Gravida 1-6
Gestational age 31 to 41 weeks
Primary postpartum hemorrhage (PPH)
Exclusion Criteria
Critically ill patients
Documented end-organ liver or renal failure (assessed by a medical record)
Documented bleeding disorder history, i.e., factor deficiencies (assessed by a medical record).
Secondary PPH
Retained products of the placenta
Chorioamnitis
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The effectiveness will be labeled as yes, where there was no blood loss for 24 hours after the removal of the pack or Foleys. Effectiveness will be labeled as failed if there was more than 100 ml of blood loss within 10 minutes after the removal of the balloon tamponade or Sengstaken-Blakemore tube. Timepoint: 24 hours. Method of measurement: Visual evidence of blood loss as per outcome measures.
- Secondary Outcome Measures
Name Time Method