Vascular Subphenotypes of Lung Disease in HIV & COPD (VAST)

This study is currently recruiting participants.

Verified April 2012 by University of Pittsburgh

Sponsor:

Information provided by (Responsible Party):

University of Pittsburgh

ClinicalTrials.gov Identifier:

NCT01581086

First received: April 17, 2012

Last updated: April 19, 2012

Last verified: April 2012

History of Changes

Purpose

This study is looking for high blood pressure in the lungs (Pulmonary artery hypertension PAH) in HIV and COPD patients.

Condition
Pulmonary Artery Hypertension

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Retrospective
Official Title:	Identify and Characterize Populations at Risk for Developing Pulmonary Arterial Hypertension (PAH)

Resource links provided by NLM:

Genetics Home Reference related topics: pulmonary arterial hypertension

MedlinePlus related topics: HIV/AIDS High Blood Pressure

U.S. FDA Resources

Further study details as provided by University of Pittsburgh:

Biospecimen Retention: Samples With DNA

Whole Blood

Estimated Enrollment:	140
Study Start Date:	January 2012
Estimated Study Completion Date:	January 2014

Eligibility

Ages Eligible for Study:	18 Years to 80 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

Pitt mens Study(MACS).

University of Pittsburgh HIV Clinic(PACT).

Emphysema COPD Research Center Research Registry(ECRC).

Criteria

Inclusion Criteria:

Male/Female 18-80 years of age.
Subject has been previously enrolled in PACT/MAC/ECRC study.
Must have recent ProBNP test >120pg/ml or abnormal echocardiogram (right ventricular systolic pressure >or=40mmHg) without evidence of left sided heart failure.

Exclusion Criteria:

Previous diagnosis of congenital heart failure.
If evidence of Left ventricular systolic or diastolic dysfunction, echo will be reviewed by the PI on a case by case basis.
Creatine clearance <60ml/min per 1.73 m2.
Undiagnosed chest pain or myocardial infarction, stroke or cardiovascular event within 3 months.
Pregnancy.
Subjects receiving chronic anticoagulant.
Inability to complete the 6 minute walk test.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01581086

Contacts

Contact: Tammi F Lawther, BS

412-624-8295

lawthertf@upmc.edu

Locations

United States, Pennsylvania
University of Pittsburgh	Recruiting
Pittsburgh, Pennsylvania, United States, 15213

Sponsors and Collaborators

University of Pittsburgh

Investigators

Principal Investigator:

Hunter C Champion, MD

University of Pittsburgh

More Information

No publications provided

Responsible Party:	University of Pittsburgh
ClinicalTrials.gov Identifier:	NCT01581086 History of Changes
Other Study ID Numbers:	VAST11060550
Study First Received:	April 17, 2012
Last Updated:	April 19, 2012
Health Authority:	United States: Institutional Review Board

Additional relevant MeSH terms:

Hypertension
Vascular Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on May 21, 2013

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