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Clinical study on cervical cerclage surgery with assisted uterine balloon filling

The efficacy and safety of a modified cervical cerclage balloon fixation with cervical clamp for the treatment of postpartum hemorrhage:A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103053
Enrollment
Unknown
Registered
2025-05-23
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Postpartum hemorrhage

Interventions

Group A Patients without cervical cerclage who require uterine balloon tamponade for postpartum hemorrhage after vaginal delivery:Patients without cervical cerclage who require uterine balloon tampona
Group B Patients with cervical cerclage requiring intrauterine balloon tamponade for postpartum hemorrhage after vaginal delivery:Patients with cervical cerclage requiring intrauterine balloon tampona

Sponsors

Maternity and Children's Hospital of Xizang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with postpartum hemorrhage after vaginal delivery requiring intrauterine balloon tamponade

Exclusion criteria

Exclusion criteria: 1 Intrauterine infection; 2 Patients who refuse to participate in the project.

Design outcomes

Primary

MeasureTime frame
Postpartum bleeding volume;Detachment of the balloon;—

Countries

China

Contacts

Public ContactBin Lv

Maternity and Children's Hospital of Xizang Autonomous Region

150022146@qq.com+86 139 8058 4568

Outcome results

None listed

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