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

Evaluation of Uterine tamponade using condom catheter balloon in management of nontraumatic postpartum hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2010/091/001054
Enrollment
15
Registered
2010-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: uterine tamponade with condom catheter balloon: 8-48 hours Control Intervention1: nil:

Sponsors

nil
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: 1. Bleeding due to genital tract trauma and retained placental tissue 2. Known allergy to latex

Design outcomes

Primary

MeasureTime frame
Success rate in controlling hemorrhageTimepoint: stable maternal condition;Time required to stop bleeding after tamponade is appliedTimepoint: control of hemorrhage—

Secondary

MeasureTime frame
Need for additional surgical measures eg devascularization ,B Lynch, hysterectomyTimepoint: unstable hemodynamic status of mother—

Countries

India

Contacts

Public ContactDr Sonali Gupta

Maulana Azad Medical College, New Delhi

asmita.rathore@yahoo.com011 28531848

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026