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| Sponsor: | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Collaborator: |
Merck |
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00720226 |
Purpose
Evidence in animals shows that losartan can prevent or reverse inflammation and lung damage due to smoking. The goal of this study is to determine whether this drug which is also used to treat hypertension can stabilize or improve lung function in people who have from chronic obstructive pulmonary disease (COPD).
| Condition | Intervention | Phase |
|---|---|---|
|
COPD Emphysema Chronic Bronchitis Smoking |
Drug: Losartan Drug: Placebo |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Efficacy of Losartan in Preventing Progression of COPD |
| Estimated Enrollment: | 120 |
| Study Start Date: | July 2008 |
| Estimated Study Completion Date: | August 2012 |
| Estimated Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Losartan 100 mg daily
|
Drug: Losartan
Losartan 100 mg daily
Other Name: Cozaar
|
|
Placebo Comparator: 2
Placebo 1 pill daily
|
Drug: Placebo
Placebo pill daily
Other Name: "Sugar pill"
|
Participants will be given either losartan in a dose of 50-100 mg per day for a period of one year. During that time, they will have lung function tests, breathing tests, and computed tomograms of the chest. These tests will determine whether there is inflammation in the lung and whether there is progressive involvement of the lung with COPD.
Eligibility| Ages Eligible for Study: | 40 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Gwen Leatherman, RN | 410 550-0800 | gleathe@jhmi.edu |
| Contact: Marie Daniels | 410 550-0800 | mdaniel@jhmi.edu |
| United States, Maryland | |
| Johns Hopkins Asthma and Allergy Center | Recruiting |
| Baltimore, Maryland, United States, 21205 | |
| Contact: Teresa Concordia, RN 410-283-5728 tconcor1@jhmi.edu | |
| Principal Investigator: Robert A. Wise, MD | |
| Sub-Investigator: Enid Neptune, MD | |
| Sub-Investigator: Nadia Hansel, MD | |
| Sub-Investigator: Gregory Diette, MD | |
| Sub-Investigator: M. Bradley Drummond, MD | |
| Principal Investigator: | Robert A. Wise, MD | Johns Hopkins University |
More Information
| Responsible Party: | Robert A. Wise, MD, Johns Hopkins University School of Medicine / Bloomberg School of Public Health |
| ClinicalTrials.gov Identifier: | NCT00720226 History of Changes |
| Other Study ID Numbers: | 1 P50 HL084945, 1 P50 HL084945 |
| Study First Received: | July 18, 2008 |
| Last Updated: | July 18, 2008 |
| Health Authority: | United States: Federal Government |
|
COPD emphysema angiotensin receptor blocker |
|
Bronchitis Bronchitis, Chronic Emphysema Pulmonary Emphysema Pulmonary Disease, Chronic Obstructive Smoking Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Tract Infections |
Pathologic Processes Habits Losartan Angiotensin Receptor Antagonists Anti-Arrhythmia Agents Cardiovascular Agents Therapeutic Uses Pharmacologic Actions Antihypertensive Agents Angiotensin II Type 1 Receptor Blockers Molecular Mechanisms of Pharmacological Action |