Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 3:22 PM
Ignite Modification Date: 2025-12-24 @ 3:22 PM
NCT ID: NCT02185092
Eligibility Criteria: Inclusion Criteria: 1. Patients admitted to OUMC or VAMC with a COPD exacerbation and pneumonia with underlying COPD will be eligible and screened. 2. Patients seen in VA Chest Medicine clinic, OU Physicians clinic and Pulmonary fellows clinic at PPOB who have had a COPD exacerbation within the last year. 3. Patients over age 18 4. Patients who have a pulmonary function test (PFT) showing COPD within 1 year of enrollment in the study or if the treating physician plans to obtain PFT as part of the patient's care plan. 5. Patients will be considered to have a diagnosis of COPD if they have a FEV1 of less than 80% of predicted and a FVC/FEV1 ratio of less than 0.70 (as defined by GOLD criteria). Exclusion Criteria: 1. Patients with less than one year of life expectancy from a concomitant diagnosis 2. Any GI motility disorders or previous bowel resection surgery (short gut syndrome) 3. Any patients with decreased immune function or on medication that may decrease immune function (other than low dose steroid or steroid taper). 4. Patients admitted within the last one year with a diagnosis of pancreatitis 5. Patients unable to give consent will not be included in the study. 6. Patients unable to sign consent 7. Patients already on azithromycin daily for COPD exacerbations 8. Patients under department of corrections custody.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 99 Years
Study: NCT02185092
Study Brief:
Protocol Section: NCT02185092