NCT Number: NCT00152984
Efficacy and Safety of Tiotropium in Patients With COPD and Concomitant Diagnosis of Asthma
The primary objective of this study is to demonstrate the superiority of tiotropium compared to placebo in the treatment of patients with COPD and a concomitant diagnosis of asthma
Looking for future studies?
Notify MeKey information
Conditions
Age range
40 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
CHU Sart Tilman, Angleur, Belgium
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Diagnosis of COPD and diagnosis of asthma before the age of 30
- Current or ex-smokers with a cigarette smoking history of at least 10 pack-years
- Treatment with inhaled steroids at least 1 year before study entry
- FEV1 increase of more than 12% 30 min. after 400 mcg salbutamol or documented reversibility of 12% documented during the past 5 years
- FEV1 increase of more than 200 mL 30 min. after 400 mcg salbutamol or documented increase of 200 mL after reversibility test within the last 5 years
- Post bronchodilator FEV1 less than 80% predicted normal (ECCS) at visit 1
- Post bronchodilator FEV1 less than 70% of FVC at visit 1
Exclusion criteria
- Respiratory infection or exacerbation 6 weeks prior to Visit 1 or during run-in period.
- Significant diseases other than COPD or asthma
- Myocardial infarction within the last 6 months
- Unstable or life-threatening cardiac arrhythmia requiring intervention or change in therapy in the last year
- Hospitalisation for heart failure (NYHA Class III or IV) within the last year
- History of life-threatening pulmonary obstruction, cystic fibrosis or clinically evident bronchiectasis
- Known active tuberculosis
- History of thoracotomy with pulmonary resection
- History of cancer within the last 5 years (excluding treated basal cell carcinoma)
- Patients requiring oxygen therapy for more than 1 hour per day
- Patients currently in a pulmonary rehabilitation programme or who have completed such a programme within 4 weeks before Visit 1
- Known hypersensitivity to anticholinergic drugs or lactose
Treatment and study plan
Placebo inhalation capsules
DrugPrimary outcomes
-
AUC(0-6) FEV1 (Area under the curve of change in FEV1 from baseline to 6 hours post dose)
Time frame: after 12 weeks of treatment
Secondary outcomes
-
Forced vital capacity (FVC)
Time frame: 12 weeks
-
Peak expiratory flow rate (PEFR)
Time frame: 12 weeks
-
Use of rescue medication
Time frame: 12 weeks
-
AUC0-6hFEV1
Time frame: after first dose on Day 1 and after 4 weeks of treatment
-
Change in trough FEV1 (i.e. trough response) from baseline.
Time frame: after 4 and 12 weeks of treatment
-
Change in peak FEV1 from baseline (=peak response) after first dose
Time frame: after 4 and 12 weeks of treatment
-
AUC0-6hFVC defined in the same way as for FEV1.
Time frame: Day 1, week 4
-
Trough FVC defined in the same way as for FEV1.
Time frame: Day 1, week 4
-
Peak FVC defined in the same way as for FEV1
Time frame: Day 1, week 4
-
Weekly average PEFR in the morning (a.m. pre-dose measurement) and in the evening (p.m. measurement).
Time frame: 12 weeks
-
Weekly average number of puffs of rescue medication used
Time frame: 12 weeks
-
Occurrence of adverse events
Time frame: 12 weeks
-
Change from baseline in pulse rate and systolic and diastolic blood pressure (seated) measured just before spirometry
Time frame: 12 weeks
-
Change from baseline in Physical examination
Time frame: 12 weeks
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Official study title
A 12-week Randomised, Double Blind, Placebo Controlled, Parallel Group Trial Evaluating the Efficacy and Safety of Inhaled Tiotropium 18μg q.d. in Patients With COPD and a Concomitant Diagnosis of Asthma
Important dates
- Study start
- 2004
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Sep 12, 2005
- Registry last updated
- Dec 28, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Generative AI for Medication Counselling and Adherence in Community Pharmacies
NCT07649577
Asthma, Bronchial Diseases
Amman, Jordan
View Trial DetailsChronical Illness-related Limitations of the Ability to Cope With Rising Temperatures, Third Wave
NCT06890208
Anxiety Disorders, Arrhythmias, Cardiac
Hamburg, Germany
View Trial DetailsDigital Tool Enhancing GPs' Information Management for Patients with Multimorbidity - a Pilot Study
NCT06061172
Asthma, Autoimmune Diseases
Hamburg, Germany
View Trial DetailsChronical Illness-related Limitations of the Ability to Cope with Rising Temperatures: an Observational Study, 2nd Wave
NCT06407154
Anxiety Disorders, Arrhythmias, Cardiac
Hamburg, Germany
View Trial Details