|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | University of British Columbia |
|---|---|
| Collaborator: |
GlaxoSmithKline |
| Information provided by: | University of British Columbia |
| ClinicalTrials.gov Identifier: | NCT00120978 |
Purpose
Large population-based studies suggest that patients with chronic obstructive pulmonary disease (COPD) are 2 to 3 times at risk for cardiovascular mortality, which accounts for a large proportion of the total number of deaths. How COPD increases the risk of poor cardiovascular outcomes is largely unknown. However, there is growing evidence that persistent low-grade systemic inflammation is present in COPD and that this may contribute to the pathogenesis of atherosclerosis and cardiovascular disease among COPD patients. Inflammation and more specifically, C-reactive protein (CRP), has been linked with all stages of atherosclerosis, including plaque genesis, rupture and subsequent thrombo-fibrosis of vulnerable vessels. Recently, our group has demonstrated in a relatively small study that short-term inhaled corticosteroid (ICS) therapy can repress serum CRP levels in stable COPD patients. Conversely, withdrawal of ICS leads to a marked increase in serum CRP levels. Although very promising, these data cannot be considered definitive because the study was small in size and scope (N=41 patients). Additionally, this study did not address the potential effects of combination therapy with ICS and long-acting β2 agonists (LABA). This is an important short-coming because combination therapy of ICS and LABA have been shown to produce improved clinical outcomes over ICS monotherapy and is commonly used by clinicians in the treatment of moderate to severe COPD. We hypothesize that inhaled fluticasone (Flovent®) reduces systemic inflammation and that combination therapy (Advair®) is more effective than steroids alone in reducing systemic inflammation in COPD. In this proposal, we will implement a randomized controlled trial to determine whether ICS by themselves or in combination with LABAs can:
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Obstructive Pulmonary Disease |
Drug: Advair Drug: Flovent |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | Advair - CRP Study |
| Estimated Enrollment: | 250 |
| Study Start Date: | December 2004 |
| Estimated Study Completion Date: | August 2006 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 45 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations| Contact: Roxanne Rousseau, BS | 604-977-9791 | RRousseau@mrl.ubc.ca |
| Contact: Don D Sin, MD | 604-806-8395 | dsin@mrl.ubc.ca |
| Canada, Alberta | |
| University of Calgary | Recruiting |
| Calgary, Alberta, Canada, T2V 1P9 | |
| Contact: Gladys Wolters, BS 403-943-3292 Gladys.Wolters@CalgaryHealthRegion.ca | |
| Principal Investigator: Gordon Ford, MD | |
| Principal Investigator: Robert Cowie, MD | |
| Wetaskiwin Lung Laboratory | Recruiting |
| Wetaskiwin, Alberta, Canada, T9A 3B8 | |
| Contact: Teena Rossiter, BS 780.352.7085 teena@incentre.net | |
| Principal Investigator: Ernest York, MD | |
| Grey Nuns Hospital | Recruiting |
| Edmonton, Alberta, Canada, T6L 5X8 | |
| Contact: Jennifer Barchard, BS 780.450.7178 JBarchar@cha.ab.ca | |
| Principal Investigator: Lyle Melenka, MD | |
| University of Alberta Hospital | Recruiting |
| Edmonton, Alberta, Canada, T6G 2B7 | |
| Contact: Heidi Haupt, BS (780) 407-7591 hhaupt@ualberta.ca | |
| Principal Investigator: Eric Wong, MD | |
| Links Clinic | Recruiting |
| Edmonton, Alberta, Canada, T5G 3G6 | |
| Contact: Jill Edwards, BS 780-913-4240 jilledwards@shaw.ca | |
| Principal Investigator: Warren Ramesh, MD | |
| Lethbridge Regional Hospital | Recruiting |
| Lethbridge, Alberta, Canada, T1J 1W5 | |
| Contact: Kathy Duce, BS 403-388-6031 kduce@mail.chr.ab.ca | |
| Principal Investigator: Eric Wilde, MD | |
| Canada, British Columbia | |
| St. Paul' Hospital | Recruiting |
| Vancouver, British Columbia, Canada, V6Z 1Y6 | |
| Contact: Roxanne Rousseau, BS 604-977-9791 RRousseau@mrl.ubc.ca | |
| Principal Investigator: Paul Man, MD | |
| Principal Investigator: Don Sin, MD | |
| Lion's Gate Hospital | Recruiting |
| North Vancouver, British Columbia, Canada, V7L 2N3 | |
| Contact: Anju Mainra, BS : 604.649.5852 mainra@shaw.ca | |
| Principal Investigator: Raj Mainra, MD | |
| Vancouver General Hospital | Recruiting |
| Vancouver, British Columbia, Canada, V5Z 3J5 | |
| Contact: Linda Hui, BS 604.875.5697 lindahui@interchange.ubc.ca | |
| Principal Investigator: Mark Fitzgerald, MD | |
| Canada, Saskatchewan | |
| Royal University Hospita | Recruiting |
| Saskatoon, Saskatchewan, Canada, S7N 0W8 | |
| Contact: Janet Baron, BS 306.966.7871 janetbaron@shaw.ca | |
| Principal Investigator: Darcy Marciniuk, MD | |
| Sub-Investigator: John Reid, MD | |
| Principal Investigator: | Don Sin, MD | University of British Columbia |
More Information
| Study ID Numbers: | SC0100141, SC0100141 |
| Study First Received: | July 11, 2005 |
| Last Updated: | May 8, 2006 |
| ClinicalTrials.gov Identifier: | NCT00120978 History of Changes |
| Health Authority: | Canada: Health Canada |
|
Clinical Trial; C-reactive protein; fluticasone; salmeterol |
|
Anti-Inflammatory Agents Respiratory System Agents Respiration Disorders Physiological Effects of Drugs Anti-Asthmatic Agents Anti-Allergic Agents Pharmacologic Actions Lung Diseases, Obstructive Respiratory Tract Diseases |
Autonomic Agents Therapeutic Uses Lung Diseases Fluticasone Peripheral Nervous System Agents Dermatologic Agents Bronchodilator Agents Pulmonary Disease, Chronic Obstructive |