Shortness Of Breath Questionnaire Validation Study
NCT00411372 · Status: WITHDRAWN · Phase: PHASE3 · Type: INTERVENTIONAL
Last updated 2015-02-23
Summary
This study will last for approximately 8 weeks and will involve 4 visits. The study is being carried out to validate a shortness of breath questionnaire
Conditions
- Pulmonary Disease, Chronic Obstructive
Interventions
- DRUG
-
fluticasone propionate/salmeterol 250/50mcg combination, salmeterol 50mcg
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
GSK Clinical Trials · GlaxoSmithKline
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-11-30
More Related Trials
-
Comparing Fluticasone-salmeterol in Chronic Obstructive Pulmonary Disease (COPD) and Sleep
NCT00731770 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of the Addition of Fluticasone Propionate/Salmeterol (250/50mcg) Twice-daily to 2 Doses of Umeclidinium Bromide Inhalation Powder (62.5 or 125mcg) Once-daily Over 12 Weeks.
NCT01772147 ·Status: COMPLETED ·Phase: PHASE3
-
Influence Of Salmeterol Xinafoate/Fluticasone Propionate (50/500 µg BID) On The Course Of The Disease And Exacerbation Frequency In COPD Patients Gold Stage III And IV
NCT00527826 ·Status: COMPLETED ·Phase: PHASE4
-
Salmeterol-Fluticasone Combined Inhaled Therapy for Non-cystic Fibrosis Bronchiectasis
NCT02782312 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation Inhaled Corticosteroids on Exhaled Nitric Oxide Gas Exchange
NCT00568347 ·Status: COMPLETED
-
Efficacy and Safety of the Addition of Fluticanse Propionate/Salmeterol (250/50mcg) Twice-daily to 2 Doses of Umeclidinium Bromide (62.5 or 125mcg) Once-daily Over 12 Weeks
NCT01772134 ·Status: COMPLETED ·Phase: PHASE3
-
Comparing Treatment Efficacy With HD/MD Flu Plus Sal in Chronic Obstructive Pulmonary Disease (COPD) Patients
NCT01131806 ·Status: UNKNOWN ·Phase: PHASE4
-
Survival Of Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT00268216 ·Status: COMPLETED ·Phase: PHASE3
-
Treatment Of Partial Reversible Chronic Obstructive Pulmonary Disease
NCT00549146 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the 24 Hour Spirometric Effect (FEV1) of Fluticasone Furoate/Vilanterol Inhalation Powder (100mcg Fluticasone Furoate (FF)/25mcg Vilanterol (VI)) Compared With Salmeterol/Fluticasone Propionate Inhalation Powder (50mcg Salmeterol/500mcg Fluticasone Propionate (FP))
NCT01342913 ·Status: COMPLETED ·Phase: PHASE3
-
Batefenterol/Fluticasone Furoate in Treatment of Chronic Obstructive Pulmonary Disease
NCT02573870 ·Status: COMPLETED ·Phase: PHASE2
-
A Dose-Finding Study Evaluating Safety and Efficacy in Patients With Chronic Obstructive Pulmonary Disease
NCT00403286 ·Status: COMPLETED ·Phase: PHASE2
-
A Study Evaluating Systemic Exposure and Pharmacodynamics in Patients With Chronic Obstructive Pulmonary Disease
NCT00774761 ·Status: COMPLETED ·Phase: PHASE2
-
A Study in Patients With Chronic Obstructive Pulmonary Disease
NCT01245569 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety Study of Formoterol/Fluticasone and Salmeterol/Fluticasone in Patients With Moderate-to-severe COPD
NCT01393145 ·Status: WITHDRAWN ·Phase: PHASE3
-
Study To Evaluate The Efficacy And Safety Of PH-797804 For 12 Weeks In Adults With Moderate To Severe Chronic Obstructive Pulmonary Disease (COPD) Taking Salmeterol Xinafoate/Fluticasone Propionate Combination
NCT01321463 ·Status: COMPLETED ·Phase: PHASE2
-
The Impact of Salmeterol-Fluticasone on Sleep in Patients With COPD
NCT00741767 ·Status: WITHDRAWN ·Phase: NA
-
Outcomes for Chronic Obstructive Pulmonary Disease Moderate Exacerbators Initiating Treatment
NCT01395875 ·Status: COMPLETED
-
Study Of Fluticasone Propionate/Salmeterol In Asthmatic Subjects
NCT00517634 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Compare Fluticasone Propionate 100mcg/Salmeterol 50 mcg Inhalation Powder to Advair Discus 100/50
NCT03562923 ·Status: UNKNOWN ·Phase: PHASE3
-
Advair® DISKUS® Versus Serevent® DISKUS® For Chronic Obstructive Pulmonary Disease Exacerbations
NCT00115492 ·Status: COMPLETED ·Phase: PHASE4
-
Fluticasone Propionate-salmeterol Combination Adherence in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01381471 ·Status: COMPLETED
-
The Efficacy and Safety of Salmeterol/Fluticasone Propionate vs Atropium/Albuterol in Patients COPD
NCT01243788 ·Status: UNKNOWN ·Phase: PHASE4
-
Effects of Inhaled Corticosteroids on Sputum Bacterial Load in COPD
NCT01213693 ·Status: COMPLETED ·Phase: NA
-
Efficacy and Safety of QMF149 vs. Salmeterol Xinafoate/Fluticasone Propionate in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01636076 ·Status: COMPLETED ·Phase: PHASE2