Skip to main content
Clinical Trials/NL-OMON23871
NL-OMON23871
Recruiting
Not Applicable

An observational study on PRegnancy outcome in women with Inherited bleeding DisordErS

niversity Medical Center Utrecht0 sites135 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
von Willebrand diseasehemophilia carrierpost partum hemorrhage (PPH)
Sponsor
niversity Medical Center Utrecht
Enrollment
135
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Ongoing pregnancy beyond 10 weeks after the last menstruation
  • \-Carrier of hemophilia A or B or Von Willebrand disease type 1, type 2 or type 3

Exclusion Criteria

  • \-Another concomitant coagulation disorder that needs a deviation of the treatment advises according to the revised national guideline on the management of pregnancy in hemophilia carriers and von Willebrand disease
  • \-Use of therapeutic or intermediate dose LMWH before delivery

Outcomes

Primary Outcomes

Not specified

Similar Trials