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Genetic Analysis of Familial Hypertrophic Cardiomyopathy

NCT00005251 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2016-03-16

No results posted yet for this study

Summary

To map the genetic defect responsible for familial hypertrophic cardiomyopathy.

Conditions

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    lead NIH

Eligibility

Max Age
100 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1990-01-31
Completion
1995-03-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00005251 on ClinicalTrials.gov