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NCT00230165Possibly a fitRecruiting

Genetics and blood testing for inherited bleeding disorders

Glanzmann Thrombasthenia

Part of Blood & lymphatic, Genetic & congenital, Heart & circulation clinical trials.

This study looks at genes and blood function in people with inherited (passed-down) problems with platelets, white blood cells, or blood clotting. It may help improve understanding of the cause of these conditions and how they work in the body.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
60 people
Ages
Any age
Study type
Observational

Who can take part

  • You must be an adult (18+) if you are enrolling as a healthy volunteer
  • You may qualify if you or a relative has an inherited platelet disorder, inherited white blood cell disorder, or inherited blood clotting disorder (including von Willebrand disease)
  • Tell the team if you have taken aspirin or similar anti-platelet medicine in the past week (it may affect results)
  • If you have donated blood recently, you may need to meet limits on how much blood you can donate in the last 8 weeks
  • If you’re a patient, your allowed blood draw depends on your recent hematocrit value (a measure in a blood test) or whether it is unknown

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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