Recruiting

Advair & Flovent

Sponsor:

University of British Columbia

Code:

NCT00120978

Conditions

Chronic Obstructive Pulmonary Disease

Eligibility Criteria

Sex: All

Age: 45+

Healthy Volunteers: Not accepted

Interventions

Advair

Flovent

Study Details

Brief summary:

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:

1. reduce CRP levels in stable COPD patients and
2. reduce other pro-inflammatory cytokines, which have been linked with cardiovascular morbidity and mortality such as interleukin-6 (IL-6) and monocyte chemoattractant protein-1 (MCP-1)

Conditions

Chronic Obstructive Pulmonary Disease

Study ID

NCT00120978

Start date

Dec, 2004

Status verified date

Apr, 2005

Completion date

Aug, 2006

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 45+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • All patients must have a clinical diagnosis of chronic obstructive pulmonary disease according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines.
  • Patients must have a cigarette smoking history of more than 10 pack-years
  • Patients must be clinically stable and at least 4 weeks from last acute exacerbation (and return to baseline level of symptoms)
  • Patients must have an FEV1 of less than 80% of predicted values with FEV1 to FVC ratio of less than 0.70 (post-bronchodilator values)
  • Men or women ≥ 45 years of age

Study Design

Enrollment

250 participants

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Interventions

Advair

Flovent

Primary outcome measure

  • Change in serum C-reactive protein levels over 3 months between treatment groups. [ Time Frame: undefined ]

Central Contacts and Locations

Central contacts

Locations

University of Calgary

Recruiting

Calgary, Alberta, Canada, T2V 1P9

Contacts

Principal Investigator:

Gordon Ford, MD

Links Clinic

Recruiting

Edmonton, Alberta, Canada, T5G 3G6

Contacts

Principal Investigator:

Warren Ramesh, MD

University of Alberta Hospital

Recruiting

Edmonton, Alberta, Canada, T6G 2B7

Contacts

Principal Investigator:

Eric Wong, MD

Grey Nuns Hospital

Recruiting

Edmonton, Alberta, Canada, T6L 5X8

Contacts

Jennifer Barchard, BS

780.450.7178JBarchar@cha.ab.ca

Principal Investigator:

Lyle Melenka, MD

Lethbridge Regional Hospital

Recruiting

Lethbridge, Alberta, Canada, T1J 1W5

Contacts

Principal Investigator:

Eric Wilde, MD

Wetaskiwin Lung Laboratory

Recruiting

Wetaskiwin, Alberta, Canada, T9A 3B8

Contacts

Principal Investigator:

Ernest York, MD

Lion's Gate Hospital

Recruiting

North Vancouver, British Columbia, Canada, V7L 2N3

Contacts

Principal Investigator:

Raj Mainra, MD

Vancouver General Hospital

Recruiting

Vancouver, British Columbia, Canada, V5Z 3J5

Contacts

Principal Investigator:

Mark Fitzgerald, MD

St. Paul' Hospital

Recruiting

Vancouver, British Columbia, Canada, V6Z 1Y6

Contacts

Principal Investigator:

Paul Man, MD

Royal University Hospita

Recruiting

Saskatoon, Saskatchewan, Canada, S7N 0W8

Contacts

Principal Investigator:

Darcy Marciniuk, MD

More Information

Sponsor

University of British Columbia

Last update posted

May 9, 2006

Last verified

Apr, 2005

Keywords

  • Clinical Trial; C-reactive protein; fluticasone; salmeterol

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of British Columbia on 2006-05-09.