Phase
Condition
Platelet Disorders
Treatment
N/AClinical Study ID
All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
A. Normal Healthy Volunteers:
Normal healthy volunteers
18 years of age or older
Either sex
Any ethnic background.
B. Patients with Glanzmann thrombasthenia or their relatives, inherited qualitative and/or quantitative platelet disorders, inherited disorders of white blood cells, inherited disorders of coagulation (including von Willebrand disease):
Adults and children
Either sex
Any ethnic background
Exclusion
Exclusion Criteria:
A. Normal Healthy Volunteers:
For studies of platelets that may be affected by anti-platelet therapy, ingestion ofaspirin or similar medication in the past week.
Having given blood in the last 8 weeks such that the current donation would exceed atotal of 250 ml for the 8 week period.
Having given blood in the past week such that this donation would result in morethan 2 donations in one week.
B. Patients with Glanzmann thrombasthenia or their relatives, inherited qualitative and/or quantitative platelet disorders, inherited disorders of white blood cells, inherited disorders of coagulation (including von Willebrand disease).
For studies of platelets that may be affected by antiplatelet therapy, ingestion ofaspirin or similar medication in the past week
If the patient is known to have a hematocrit ≥25 (assay performed in past 3 months),the same blood drawing criteria as in A, with the addition that for children lessthan 18 years of age, the maximum amount of blood allowed to be donated in an 8 weekperiod is the lesser of 50 ml or 3 ml/kg.
If the patient has a hematocrit <25 or if the hematocrit is unknown, the blooddrawing limit is the lesser of 20 ml or 1 ml/kg in any 8 week period.
Study Design
Study Description
Connect with a study center
Rockefeller University Hospital
New York, New York 10021
United StatesActive - Recruiting
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