ACTRN12615000076572
Not yet recruiting
未知
The Effects of One Month of Therapy with the Long-acting Bronchodilator Tiotropium on Ventilation Heterogeneity in Patients with Chronic Obstructive Pulmonary Disease
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Woolcock Institute of Medical Research
- Enrollment
- 45
- Status
- Not yet recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Adults with physician\-diagnosed mild\-moderate chronic obstructive pulmonary disease, with history of current or past smoking (total exposure \> 10 pack years)
Exclusion Criteria
- •\* Use of tiotropium or any other LAMA or LABA within the previous 4 weeks
- •\* Musculoskeletal (for example, severe arthritis) or other conditions which limit the ability to walk at near\-maximal pace
- •\* Significant cardiac disease (ischaemic heart disease or arrhythmia) deemed by the investigators or the subject’s treating cardiologist to make it unsafe for the subject to undertake a supervised near\-maximal exercise test
- •\* Documented hypersensitivity to, or intolerance of, anti\-cholinergic therapies
- •\* Significant respiratory infection or documented exacerbation of COPD within the previous 6 weeks
- •\* Other active or chronic respiratory pathologies (for example, interstitial lung disease, asthma, chest wall pathology causing ventilatory restriction)
- •\* Past history of lung surgery (including lobectomy or pneumonectomy, but not lung biopsy) or thoracic radiation therapy (excluding isolated mediastinal radiation therapy with no evidence of subsequent pulmonary fibrosis)
- •\* Any major comorbidities deemed to impact on respiratory physiology or symptoms, including severe on uncontrolled heart failure, morbid obesity, muscular or neurological disorders causing respiratory muscle weakness or dysfunctional swallowing
- •\* History of chronic kidney disease (moderate to severe, eGFR less than or equal to 45 mL/min/1\.73m2\) or severe hepatic impairment
- •\* Unable to perform lung function testing at the enrollment visit
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, not recruiting
Not Applicable
Evaluation of the effect of 6 months treatment with V0191 on symptoms changes in patients with Mild Cognitive Impairment. Multicentre, randomised, double-blind, placebo-controlled study in parallel groups.EUCTR2007-001975-12-BEPIERRE FABRE MEDICAMENT - IDPF200
Active, not recruiting
Not Applicable
Evaluation of the effect of 6 months treatment with V0191 on symptoms changes in patients with Mild Cognitive Impairment. Multicentre, randomised, double-blind, placebo-controlled study in parallel groups.Mild Cognitive ImpairmentMedDRA version: 9.1Level: LLTClassification code 10009846Term: Cognitive impairmentEUCTR2007-001975-12-FIPIERRE FABRE MEDICAMENT - IDPF210
Active, not recruiting
Phase 1
Evaluation of the effect of 6 months treatment with V0191 on symptoms changes in patients with Mild Cognitive Impairment. Multicentre, randomised, double-blind, placebo-controlled study in parallel groups.Mild Cognitive ImpairmentMedDRA version: 9.1Level: LLTClassification code 10009846Term: Cognitive impairmentEUCTR2007-001975-12-FRPIERRE FABRE MEDICAMENT - IDPF200
Active, not recruiting
Phase 1
Evaluation of the effect of 6 months treatment with DC158AM on fatigue in patients with Parkinson’s disease. Multicentre, randomised, double-blind, placebo-controlled study in parallel groups.Fatigue symptoms in Parkinson's disease.MedDRA version: 9.1 Level: LLT Classification code 10013113 Term: Disease Parkinson'sEUCTR2007-002195-34-FRPIERRE FABRE MEDICAMENT120
Active, not recruiting
Not Applicable
Evaluation of the effect of 6 months treatment with V0191 on symptoms changes in patients with Mild Cognitive Impairment. Multicentre, randomised, double-blind, placebo-controlled study in parallel groups.EUCTR2007-001975-12-ATPIERRE FABRE MEDICAMENT - IDPF210