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NCT00156429

Genetic Predictors of Outcome in HCM Patients

Terminated Last updated 4 August 2020
What this trial tests

trial in Hypertrophic Cardiomyopathy in 98 participants. Terminated before completion.

Timeline
22 April 2009
Primary endpoint
30 July 2020
30 July 2020

Quick facts

Lead sponsorUniversity of Pittsburgh
StatusTerminated
Study typeOBSERVATIONAL
Enrollment98
Start date22 April 2009
Primary completion30 July 2020
Estimated completion30 July 2020
Sites1 location across United States

Conditions studied

Sponsor

University of Pittsburgh

Who can join

18 and older, any sex, with Hypertrophic Cardiomyopathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a retrospective review of the data available on patients and their family members with HCM and prospective follow-up of this cohort for clinical outcome and diagnostic studies. Genetic samples are being examined in this cohort to determine whether certain to determine whether certain beta-AR polymorphisms as well as other common genetic polymorphisms are associated with different morphological features, such as LVH in patients with HCM and whether these polymorphisms influence the clinical course and outcome in patients with HCM. For that purpose, we will build a database with clinical information including serial echocardiographic measurements for patients with HCM that have regular follow up and test them for beta-AR polymorphisms as well as other common genetic polymorphisms and other known cardiac-related polymorphisms that can potentially contribute to the morphologic differences seen in patients with HCM.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hypertrophic Cardiomyopathy

Currently open trials in the same condition.

Other University of Pittsburgh trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing