SCCOR Minorities Observational Study

Pulmonary Disease, Chronic Obstructive Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02898272
• Other study ID #: PRO16040015
• Status: Completed
• Start date: August 2016
• Est. completion date: March 31, 2023

Study information

• Verified date: May 2023
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The SCCOR Minorities study will recruit minority participants from the COPDGene cohort, in whom the University of Pittsburgh has already obtained baseline and five year data, in order to enhance bone mineral density and vascular function data collection from minority smokers. Dual X-ray absorptiometry (DXA) scans will be obtained to measure bone mineral density. Non-invasive vascular studies will be performed to measure endothelial function. Questionnaires regarding symptoms and activity levels will be administered and a blood sample will be obtained in participants in which blood samples are not already available from the COPDGene study visits.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: March 31, 2023
• Est. primary completion date: March 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 80 Years

Eligibility

Inclusion Criteria:

• African American male and female subjects participating in COPDGene study

Exclusion Criteria:

• caucasians

• pregnant women

Related Conditions & MeSH terms

• Emphysema
• Pulmonary Disease, Chronic Obstructive

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Pittsburgh

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dual Xray Absorptiometry measurement of lumbar spine and hip bone mineral density.		As this is a cross-sectional collection of data, the outcome will be measured once at the first and only study visit.
Secondary	Measurement of carotid artery intimal thickness with ultrasound		As this is a cross-sectional collection of data, the outcome will be measured once at the first and only study visit.