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The comparative study to evaluate the success rate of the intrauterine tamponade balloon and gauze packing the event of uncontrollable hemorrhage due to Placenta Previa in Cesarean Section cases: a randomized perspective controlled multicenter trial

The comparative study to evaluate the success rate of the intrauterine tamponade balloon and gauze packing the event of uncontrollable hemorrhage due to Placenta Previa in Cesarean Section cases: a randomized perspective controlled multicenter trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15006467
Enrollment
Unknown
Registered
2015-05-29
Start date
2015-06-01
Completion date
Unknown
Last updated
2018-01-22

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

Conditions

placenta previa

Interventions

A :intrauterine inflated balloon
B :gauze packing

Sponsors

Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Term gestation (>=28weeks); 2. placenta previa of CS; 3. failed of the first line therapy; 4. patient agreed.

Exclusion criteria

Exclusion criteria: 1. previa accred; 2. uterus infection; 3. others.

Design outcomes

Primary

MeasureTime frame
the rate of successful hemostasis;the average amount of 24 hours PPH;intrauterine infection;The average postoperative pain score;—

Secondary

MeasureTime frame
puerperium complication .;—

Countries

China

Contacts

Public ContactYali Hu

Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School

glyyhuyali@163.com+86 13951846008

Outcome results

None listed

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