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Completed

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

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

CHU Sart Tilman, Angleur, Belgium

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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

Tiotropium inhalation capsules

Drug

Placebo inhalation capsules

Drug

Primary outcomes

  1. 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

  1. Forced vital capacity (FVC)

    Time frame: 12 weeks

  2. Peak expiratory flow rate (PEFR)

    Time frame: 12 weeks

  3. Use of rescue medication

    Time frame: 12 weeks

  4. AUC0-6hFEV1

    Time frame: after first dose on Day 1 and after 4 weeks of treatment

  5. Change in trough FEV1 (i.e. trough response) from baseline.

    Time frame: after 4 and 12 weeks of treatment

  6. Change in peak FEV1 from baseline (=peak response) after first dose

    Time frame: after 4 and 12 weeks of treatment

  7. AUC0-6hFVC defined in the same way as for FEV1.

    Time frame: Day 1, week 4

  8. Trough FVC defined in the same way as for FEV1.

    Time frame: Day 1, week 4

  9. Peak FVC defined in the same way as for FEV1

    Time frame: Day 1, week 4

  10. Weekly average PEFR in the morning (a.m. pre-dose measurement) and in the evening (p.m. measurement).

    Time frame: 12 weeks

  11. Weekly average number of puffs of rescue medication used

    Time frame: 12 weeks

  12. Occurrence of adverse events

    Time frame: 12 weeks

  13. Change from baseline in pulse rate and systolic and diastolic blood pressure (seated) measured just before spirometry

    Time frame: 12 weeks

  14. 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.

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