Molecular Biology of Polycythemia and Thrombocytosis

Recruiting now

Conditions studied: Polycythemia, Thrombocytosis

In brief

Our study is designed to characterize the clinical picture and genetic pattern of Polycythemia and Thrombocytosis. The purpose of this project is to find a gene and its mutation that causes these disorders. When this is accomplished, new therapies to control and eventually cure the disorder can be designed.

Key facts

Study ID

NCT00722527

Run by

University of Utah

People needed

200

Starts

2006-07-01

Expected to finish

2028-07-01

Last updated by the study team

2026-03-09

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with an elevated hemoglobin concentration (>18 in males and >16 in females)
• Subjects with an elevated platelet count (>450,000)

You may not qualify if…

• Subjects who have a known acquired cause of polycythemia and thrombocytosis
• Subjects with heart disease, left to right heart shunt or severe pulmonary disease

Where it is running

• University of Utah — Salt Lake City, Utah, United States (enrolling)

Full record on ClinicalTrials.gov

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