FindTrial
Sign In

Balloon tamponade for non-traumatic postpartum hemorrhage

Balloon tamponade for non-traumatic postpartum hemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-15006084
Enrollment
Unknown
Registered
2015-03-12
Start date
2015-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Postpartum hemorrhage

Interventions

Case series:intra-uterine balloon tamponade

Sponsors

Nanjing Drum Tower Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Vaginal delivery with blood loss >500ml, failure to react to uterotonics, non-traumatic hemorrhage; 2.Cesarean delivery with blood loss >1000ml, non-traumatic hemorrhage; 3.Postpartum hemorrhage waiting for DSA uterine artery embolisation; 4.Postpartum hemorrhage with coagulation defect to decrease blood loss; 5.Preventive use of intra-uterine balloon tamponade in placenta previa; 6.Informed consent.

Exclusion criteria

Exclusion criteria: 1.Postpartum hemorrhage with birth canal laceration; 2.Uterine anormality; 3.Suspected severe intra-uterine infection; 4.Uterine rupture.

Design outcomes

Primary

MeasureTime frame
Postpartum blood loss;Blood transfusion volume;Success Rate of hemostasis;—

Secondary

MeasureTime frame
Blood Pressure;Heart Rate;Hemoglobin;Thrombin time;Activated partial thromboplastin time;VAS score;—

Contacts

Public ContactHu Yali
glyyhuyali@163.com+86 13951846008

Outcome results

None listed

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