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Familial Myeloproliferative Disorders

NCT00666289 · View on ClinicalTrials.gov ↗

Study Summary

Myeloproliferative disorders occur in families, thus giving rise to the theory that it is a genetic disease that may be caused by an abnormal gene in the DNA that can be passed from one generation of family members to another. DNA can be gathered from family members through blood samples and the investigators will investigate (through DNA testing) to see if there are abnormal genes that may be responsible for causing the MPDs. Understanding which genes are responsible for causing MPDs can help develop ways to identify people who may be at risk for developing an MPD, allow for the development of better treatments, possibly a cure, or even prevent the development of MPDs.

Study Locations (6)

New York

  • Mount Sinai School of Medicine — New York
  • Weill Cornell — New York

District of Columbia

  • Georgetown University — Washington D.C.

Illinois

  • University of Illinois at Chicago — Chicago

Utah

  • University of Utah — Salt Lake City

Other

  • University of Florence — Florence

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2008-03
Est. Completion 2015-06-20

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00666289

The ClinicalTrials.gov registry entry for NCT00666289 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 946 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Polycythemia Vera appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00666289 reports 6 study locations spanning 5 distinct geographic areas — top geographies include New York, District of Columbia, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00666289 about?

NCT00666289 is a clinical study titled "Familial Myeloproliferative Disorders". Myeloproliferative disorders occur in families, thus giving rise to the theory that it is a genetic disease that may be caused by an abnormal gene in the DNA that can be passed from one generation of family members to another. DNA can be gathered from family members through blood samples and the inv...

What is the current status of trial NCT00666289?

This trial is currently completed. The enrollment target is 17 participants. The study started on 2008-03. Estimated completion is 2015-06-20.

What conditions does trial NCT00666289 study?

This clinical trial studies the following conditions: Polycythemia Vera, Essential Thrombocythemia, Idiopathic Myelofibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT00666289?

This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 946 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00666289 being conducted?

This trial has 6 study locations across District of Columbia, Illinois, New York, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial