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NCT02604602 Clinical Trial

Coagulation Factors and Postpartum Hemorrhage

Postpartum Hemorrhage Clinical Trial

Official title:
Peripartal Concentration of Coagulation Factors and Postpartum Hemorrhage

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02604602
Other study ID # KEK-ZH-Nr. 2015-0011
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2015
Est. completion date April 20, 2020

Study information
Verified date April 2020
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Objective is to analyze a possible association of coagulation factors peripartal with the occurrence of postpartum hemorrhage.

Recruitment information / eligibility
Status Completed
Enrollment 1500
Est. completion date April 20, 2020
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- pregnant women > 22 weeks of gestation

Exclusion Criteria:

- age < 18 years, no informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• blood exam
laboratory test

Locations
Country Name City State
Switzerland University Hospital of Zurich Zurich

Sponsors (1)
Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary occurrence of PPH 7 days
See also
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Recruiting NCT05382403 - Novel Vacuum-Induced Hemorrhage Control for Postpartum Hemorrhage N/A
Not yet recruiting NCT02853552 - Misoprostol as First Aid Measure to Address Excessive Postpartum Bleeding Phase 4
Completed NCT03344302 - Oxytocin Administration During Cesarean Section Phase 4
Completed NCT02805426 - Effectiveness of Tranexamic Acid When Used as an Adjunct to Misoprostol for the Treatment of Postpartum Hemorrhage Phase 4