A study of Condom catheter balloon to control excessive bleeding after childbirth.

• Conditions: postpartum hemorrhage

• Registration Number: CTRI/2010/091/001054

Brief Summary

tamponade created at predefined point. Primary outcomes noted. If successful, tamponade continued for 8-48 hours with defined monitoring. Tamponade removed after criterias fulfilled. Secondary outcomes noted.

Detailed Description

Not available

Recruitment & Eligibility

• Sex: Not specified
• Target Recruitment: 15

Inclusion Criteria

Post partum hemorrhage not responding to medical management (appropriate doses of oxytocics and prostaglandins).

Exclusion Criteria

• Bleeding due to genital tract trauma and retained placental tissue2.
• Known allergy to latex.

Study & Design

• Study Type: Not specified
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time required to stop bleeding after tamponade is applied	control of hemorrhage

Secondary Outcome Measures

Name	Time	Method
Need for additional surgical measures eg devascularization ,B Lynch, hysterectomy	unstable hemodynamic status of mother

Trial Locations

Locations (1)

Department of obstetrics and gynecology, Maulana Azad Medical College, NewDelhi; 🇮🇳 India

Department of obstetrics and gynecology, Maulana Azad Medical College, NewDelhi

🇮🇳India

Dr A M Rathore

Principal investigator

09968604345

asmita.rathore@yahoo.com