FindTrial
Sign In

Clinical study on the prevention of postpartum hemorrhage with calcium gluconate

Clinical study on the prevention of postpartum hemorrhage with calcium gluconate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104481
Enrollment
Unknown
Registered
2025-06-18
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-06-24

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 :Intravenous infusion of calcium gluconate after umbilical cord transection
Group B :No need for calcium gluconate after umbilical cord transection

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 after vaginal delivery and cesarean section

Exclusion criteria

Exclusion criteria: 1. Pregnancy induced hypertension; 2. Patients who refuse to participate in the project.

Design outcomes

Primary

MeasureTime frame
2-hour postpartum bleeding volume;24-hour postpartum bleeding volume;—

Secondary

MeasureTime frame
Postpartum hemoglobin changes;Intraoperative blood transfusion volume;—

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