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Identification of Genetic Markers for Cardiopulmonary Diseases (Genotype)

NCT00616369 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 255

Last updated 2016-01-11

No results posted yet for this study

Summary

This study is designed to investigate whether an association exists between certain genes/protein levels and the development of various cardiopulmonary diseases. It is hoped that this project will provide valuable insight into the understanding of these diseases.

Conditions

Sponsors & Collaborators

  • University of Alabama at Birmingham

    lead OTHER

Principal Investigators

  • Robert C Bourge, MD · University of Alabama at Birmingham Division of Medicine

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2015-01-31
Completion
2015-01-31

Countries

  • United States

Study Locations

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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 NCT00616369 on ClinicalTrials.gov