The Effect of Fluticasone/Salmeterol Combination on Exertional Breathlessness in Patients With Mild COPD - Full Text View

Sponsors and Collaborators:	Queen's University GlaxoSmithKline
Information provided by:	Queen's University
ClinicalTrials.gov Identifier:	NCT00559312

Purpose

Even patients with milder COPD can have significant physiological abnormalities which become more pronounced during exercise, leading to intolerable breathing discomfort (dyspnea). While there is a compelling physiological rationale for the efficacy of inhaled corticosteroid/long-acting bronchodilator combination therapy [i.e., fluticasone 250μg/salmeterol 50μg (FSC250/50)] in moderate to severe COPD, little information is available on the potential impact of this therapy in milder symptomatic disease. This study will be the first to explore mechanisms of dyspnea and activity limitation in milder COPD and will determine if there is a sound physiological rationale for the use of FSC as therapy for this subpopulation.

Condition	Intervention
COPD	Drug: fluticasone/salmeterol combination Drug: placebo

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Crossover Assignment, Efficacy Study
Official Title:	A 6-Week Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Assess the Effect of Fluticasone 250μg/Salmeterol 50μg Combination (FSC 250/50) on Exertional Dyspnea in Patients With Symptomatic Mild COPD

Resource links provided by NLM:

MedlinePlus related topics: Breathing Problems Exercise and Physical Fitness

Drug Information available for: Fluticasone propionate Salmeterol Fluticasone Salmeterol xinafoate

U.S. FDA Resources

Further study details as provided by Queen's University:

Primary Outcome Measures:

Dyspnea intensity (Borg rating at a standardized time during exercise) [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

Exercise endurance time [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
Measurements of small airway function [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
Exercise measurements of ventilation, breathing pattern, operating lung volumes and respiratory mechanics [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment:	40
Study Start Date:	December 2007
Estimated Study Completion Date:	December 2009
Estimated Primary Completion Date:	December 2009 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
1: Experimental fluticasone 250μg/salmeterol 50μg combination	Drug: fluticasone/salmeterol combination Diskus inhaler, fluticasone 250μg/salmeterol 50μg, twice daily, 6-week duration
2: Placebo Comparator matched placebo inhaler	Drug: placebo Placebo Diskus inhaler, twice daily, 6-week duration

Eligibility

Ages Eligible for Study:	41 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Stable mild COPD,
FEV1/FVC<0.7 and FEV1>60% predicted,
Baseline Dyspnea Index focal score <9 and MRC dyspnea scale >2,
Cigarette smoking history ≥20 pack-years.

Exclusion Criteria:

Presence of a significant disease other than COPD that could contribute to dyspnea and exercise limitation,
Important contraindications to clinical exercise testing,
Use of daytime oxygen,
History of Asthma.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00559312

Contacts

Contact: Katherine A Webb, M.Sc.

(613) 549-6666 ext 4950

kw2@queensu.ca

Locations

Canada, Ontario
Respiratory Investigation Unit at Kingston General Hospital	Recruiting
Kingston, Ontario, Canada, K7L 2V7
Principal Investigator: Denis E O'Donnell, MD, FRCPC

Sponsors and Collaborators

Queen's University

GlaxoSmithKline

Investigators

Principal Investigator:

Denis E O'Donnell, MD, FRCPC

Queen's University and Kingston General Hospital

More Information

No publications provided

Responsible Party:	Queen's University ( Dr. Denis O'Donnell )
Study ID Numbers:	SCO110755
Study First Received:	November 14, 2007
Last Updated:	April 16, 2009
ClinicalTrials.gov Identifier:	NCT00559312 History of Changes
Health Authority:	Canada: Ethics Review Committee

Keywords provided by Queen's University:

mild COPD
dyspnea
exercise
combination therapy

Study placed in the following topic categories:

Anti-Inflammatory Agents
Neurotransmitter Agents
Salmeterol
Adrenergic Agents
Adrenergic beta-Agonists
Albuterol
Anti-Asthmatic Agents
Anti-Allergic Agents
Adrenergic Agonists

Lung Diseases, Obstructive
Respiratory Tract Diseases
Lung Diseases
Fluticasone
Peripheral Nervous System Agents
Dyspnea
Bronchodilator Agents
Pulmonary Disease, Chronic Obstructive

Additional relevant MeSH terms:

Anti-Inflammatory Agents
Respiratory System Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Albuterol
Physiological Effects of Drugs
Reproductive Control Agents
Adrenergic Agonists
Lung Diseases, Obstructive
Respiratory Tract Diseases
Tocolytic Agents
Therapeutic Uses

Fluticasone
Dermatologic Agents
Salmeterol
Adrenergic beta-Agonists
Anti-Asthmatic Agents
Anti-Allergic Agents
Pharmacologic Actions
Autonomic Agents
Lung Diseases
Peripheral Nervous System Agents
Bronchodilator Agents
Pulmonary Disease, Chronic Obstructive

ClinicalTrials.gov processed this record on July 02, 2009