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Clinical Trials/NL-OMON47172
NL-OMON47172
Completed
Not Applicable

I-chec - Identifying children with hereditary coagulation disorders - I-chec

Academisch Medisch Centrum0 sites50 target enrollmentTBD
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Conditionscoagulation disorderInherited bleeding disorder1006447710005330

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
coagulation disorder
Sponsor
Academisch Medisch Centrum
Enrollment
50
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Age 0\-18 years
  • •2\. Presenting with (1\) the history, signs and symptoms of bleeding, and/or (2\) abberant laboratory blood parameters and/or (3\) a diagnosis of a bleeding disorder in relatives

Exclusion Criteria

  • •1\. Patients with a previous diagnosis of an inherited bleeding disorder
  • •2\. Patients with a known, acquired cause of bleeding (ie. renal or liver disease, use of medication that is known to cause an increased bleeding tendency)

Outcomes

Primary Outcomes

Not specified

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