Hunting the gene behind blood disorders

NCT ID NCT00722527

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is looking for the genetic mutation that causes polycythemia (too many red blood cells) and thrombocytosis (too many platelets). Researchers will analyze blood samples from 200 participants to identify the faulty gene. Finding this gene could help design new treatments to control or even cure these conditions in the future.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to
If successful, this research could identify the genetic mutation causing these blood disorders, paving the way for future targeted therapies.
What could go wrong
This is an observational study, not a treatment trial. Finding the genetic cause does not guarantee that effective treatments will be developed.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

Hypoxia polycythemia Polycythemia, primary familial and congenital thrombocytosis disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University of Utah

    RECRUITING

    Salt Lake City, Utah, 84132, United States

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Other studies related to the condition(s) this trial covers.