Impact of Fluticasone and Salmeterol on Airway Dendritic Cells (DCs) in Smokers
NCT00908362 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 45
Last updated 2010-01-13
Summary
Airway dendritic cells (DCs) play a key role in smoke-related lung diseases. In this study, the researchers investigate the effects of fluticasone and salmeterol on human airway DCs in smokers. The researchers hypothesize that fluticasone and salmeterol impact on the number and the characteristics of airway DCs in smokers.
Conditions
- Smoke-related Lung Diseases
- Chronic Obstructive Pulmonary Disease
Interventions
- DRUG
-
fluticasone
Participants inhale fluticasone (250 µg) via discus. Before and after this therapy, a bronchoalveolar lavage is performed.
- DRUG
-
fluticasone/salmeterol
Participants inhale fluticasone/salmeterol (250/50µg) via discus. Before and after this therapy, a bronchoalveolar lavage is performed.
- DRUG
-
Participants inhale placebo twice daily via discus. Before and after this therapy, a bronchoalveolar lavage is performed.
Sponsors & Collaborators
- collaborator INDUSTRY
-
University of Rostock
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 30 Years
- Max Age
- 60 Years
- Sex
- MALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-05-31
- Primary Completion
- 2009-10-31
- Completion
- 2009-12-31
Countries
- Germany
Study Locations
More Related Trials
-
The Effect of Fluticasone/Salmeterol Combination on Exertional Breathlessness in Patients With Mild COPD
NCT00559312 ·Status: COMPLETED ·Phase: NA
-
Evaluation Of Patient Satisfaction Of Metered Dose Inhaler (MDI) With Counter In Asthmatics And Chronic Obstructive Pulmonary Disease Patients (COPD).
NCT00404261 ·Status: COMPLETED ·Phase: PHASE4
-
A Trial to Assess the Pharmacodynamic Response in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT01168310 ·Status: COMPLETED ·Phase: PHASE2
-
Effects of Inhaled Corticosteroids on Sputum Bacterial Load in COPD
NCT01213693 ·Status: COMPLETED ·Phase: NA
-
Airway Hyper-responsiveness Study In Asthma Using Salmeterol/Fluticasone Propionate Combination Product
NCT00291382 ·Status: COMPLETED ·Phase: PHASE4
-
Airway Inflammation In Patients With Chronic Obstructive Pulmonary Disease
NCT00268177 ·Status: COMPLETED ·Phase: PHASE3
-
A Dose-Finding Study Evaluating Safety and Efficacy in Patients With Chronic Obstructive Pulmonary Disease
NCT00403286 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical Study Evaluating Safety and Efficacy of Fluticasone Furoate and Fluticasone Propionate in People With Asthma
NCT01436110 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Efficacy and Safety of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT01009463 ·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
-
Outcomes for Chronic Obstructive Pulmonary Disease Moderate Exacerbators Initiating Treatment
NCT01395875 ·Status: COMPLETED
-
Study to Evaluate the Effect of Fluticasone Furoate/Vilanterol on Survival in Subjects With Chronic Obstructive Pulmonary Disease
NCT01313676 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate the 24-Hour Pulmonary Function Profile of Fluticasone Furoate/Vilanterol (FF/VI) Inhalation Powder 100/25mcg Once Daily Compared With Tiotropium Bromide Inhalation Powder 18mcg Once Daily in Subjects With COPD Who Have or Are At Risk for Co-morbid Cardiovascular Disease
NCT01627327 ·Status: COMPLETED ·Phase: PHASE3
-
Flutiform® Compared With Seretide® in the Treatment of COPD
NCT02195375 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Comparing Fluticasone-salmeterol in Chronic Obstructive Pulmonary Disease (COPD) and Sleep
NCT00731770 ·Status: COMPLETED ·Phase: PHASE4
-
Special Drug Use Investigation for ADOAIR DISKUS COPD (Salmeterol and Fluticasone)
NCT01332409 ·Status: COMPLETED
-
Randomized Trial of Fluticasone in Bronchial Premalignancy
NCT00407264 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Compare Fluticasone Propionate 100mcg/Salmeterol 50 mcg Inhalation Powder to Advair Discus 100/50
NCT03562923 ·Status: UNKNOWN ·Phase: PHASE3
-
A Long-term Safety Study of Fluticasone Furoate (FF)/GW642444 in Japanese Subjects With COPD
NCT01192191 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT01017952 ·Status: COMPLETED ·Phase: PHASE3
-
Enhancement of in-Vitro GC Function in Patients With COPD
NCT00241631 ·Status: COMPLETED ·Phase: PHASE2
-
Budesonide / Formoterol in Treatment of Exacerbations of COPD
NCT00239278 ·Status: COMPLETED ·Phase: PHASE2
-
Study Of Fluticasone Propionate/Salmeterol In Asthmatic Subjects
NCT00517634 ·Status: COMPLETED ·Phase: PHASE4
-
Repeat Dose Study of Fluticasone Propionate/Salmeterol Versus Fluticasone Propionate + Salmeterol In Asthmatics
NCT00364442 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy and Safety Study of Fluticasone Furoate (FF)/GW642444 Inhalation Powder and the Individual Components in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT01054885 ·Status: COMPLETED ·Phase: PHASE3