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A Registry of COPD Patients to be Used for Future Studies

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ClinicalTrials.gov Identifier: NCT00814203
Recruitment Status : Unknown
Verified April 2015 by Philip Diaz, The Ohio State University.
Recruitment status was:  Recruiting
First Posted : December 24, 2008
Last Update Posted : April 21, 2015
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
To develop a cohort of COPD participants to assist study staff in determining the most likely candidates for future studies.

Condition or disease
Chronic Obstructive Lung Disease

Detailed Description:
To develop a cohort of COPD participants for study staff to determine the most likely candidates for future studies and to develop a repository of blood from subjects with COPD for future studies.

Study Design

Study Type : Observational
Estimated Enrollment : 600 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: The Ohio State University COPD Registry
Study Start Date : December 2008
Estimated Primary Completion Date : December 2015
Estimated Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: COPD Lung Diseases
U.S. FDA Resources

Groups and Cohorts

Group/Cohort
Chronic obstructive lung disease
those with a condition


Outcome Measures

Primary Outcome Measures :
  1. This is a registry protocol to determine factors contributing to the development of chronic obstructive lung disease.

Secondary Outcome Measures :
  1. To develop a repository of blood from subjects with COPD for future studies. These studies may include evaluation of biologic markers of disease severity and progression.

Biospecimen Retention:   Samples With DNA
whole blood

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
primary care clinic
Criteria

Inclusion Criteria:

  • Patients who are 18 years of age and older who have been diagnosed with COPD by at least one of the following:

    • clinical history-a documented history of COPD, emphysema, or chronic bronchitis;
    • pulmonary function results (defined as an FEV1/FVC less than 0.7;
    • radiographic results (high-resolution CT findings of emphysema

Exclusion Criteria:

  • in ability to give informed consent
  • prisoners
  • pregnancy
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00814203


Contacts
Contact: Janice E Drake, CRTT 614-366-2287 janice.drake@osumc.edu
Contact: Sharon T Cheung, BS 614-366-2258 sharon.cheung@osumc.edu

Locations
United States, Ohio
The Ohio State University Recruiting
Columbus, Ohio, United States, 43210
Principal Investigator: Philip T Diaz, MD         
Sub-Investigator: Michael E Ezzie, MD         
Sub-Investigator: Clay B Marsh, MD         
Sponsors and Collaborators
Philip Diaz
Investigators
Principal Investigator: Philip Diaz, MD Ohio State University
More Information

Responsible Party: Philip Diaz, Philip Diaz M.D., The Ohio State University
ClinicalTrials.gov Identifier: NCT00814203     History of Changes
Other Study ID Numbers: 2007H0248
First Posted: December 24, 2008    Key Record Dates
Last Update Posted: April 21, 2015
Last Verified: April 2015

Keywords provided by Philip Diaz, The Ohio State University:
COPD

Additional relevant MeSH terms:
Lung Diseases
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Respiratory Tract Diseases