Expired Study
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Buffalo, New York 14215


Purpose:

This is an eight-week, randomized, controlled, two arm parallel study. The study consists of, a screening visit, two weeks of intervention-free run-in randomization, clinic visits week 0, 1, 2, 4, 6, and 8 weeks during the intervention period to collect 24 hour sputum and to confirm techniques of device use and entries into daily diaries. Twenty-four (24) hour sputum samples will be collected and weighed at each clinic visit. In addition to clinic visits, subjects will be expected to make daily diary entries of COPD symptoms. Clinical evaluation will include adverse event surveillance, and St. Georges Respiratory questionnaire.


Study summary:

No further details


Criteria:

Inclusion Criteria: - Age of over 40 with COPD Exclusion Criteria: - Children, - New mothers; and - Women intending to become pregnant


NCT ID:

NCT00560105


Primary Contact:

Principal Investigator
Sanjay Sethi, MD
VA Western NY Healthcare System


Backup Contact:

N/A


Location Contact:

Buffalo, New York 14215
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 22, 2017

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