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A Multi-center study for early bundel resuscitation of postpartum hemorrhage

A Multi-center study for early bundel resuscitation of postpartum hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022604
Enrollment
Unknown
Registered
2019-04-18
Start date
2019-04-17
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Postpartum Hemorrhage

Interventions

Control group:Traditional recovery programs
Experimental group:Bundel recovery programs

Sponsors

Dalian Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients with more than 1500ml of blood loss at 24h or more than 1500ml of total blood transfusion products or hemorrhagic shock.

Exclusion criteria

Exclusion criteria: Postpartum hemorrhage patients with diseases that affect blood clotting (Hemophilia, Vitamin K Deficiency, Hemophilia, Disseminated Intravascular Coagulation, and Severe Liver Disease) are excluded.

Design outcomes

Primary

MeasureTime frame
Blood transfusion volume;Bleeding volume;Blood coagulation function;Mortality;—

Countries

China

Contacts

Public ContactYang Rongli
yever3000@yeah.net+86 15904963796

Outcome results

None listed

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