Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Free Combinations of Tiotropium Inhalation Powder Capsule + Salmeterol Metered Dose Inhaler, Tiotropium Inhalation Powder Capsule and Salmeterol Metered Dose Inhaler in Patients With Chronic Obstructive Pulmonary Disease (COPD)

16 settembre 2014 aggiornato da: Boehringer Ingelheim

A Randomised, Double-blind, Double-dummy, Crossover Efficacy and Safety Comparison of 6-week Treatment Periods of the Free Combinations of Tiotropium Inhalation Powder Capsule (18 μg) QD + Salmeterol Metered Dose Inhaler (2 Puffs of 25 μg) QD or BID, Tiotropium Inhalation Powder Capsule (18 μg) QD and Salmeterol Metered Dose Inhaler (2 Puffs of 25 μg) BID in Patients With (COPD)

Main Study: To evaluate and to compare the lung function response to the free combinations of tiotropium 18 μg (QD) + salmeterol 50 μg (QD or BID), salmeterol 50 μg BID and tiotropium 18 μg QD at the end of 6-week treatment periods in patients with COPD.

Sub-Study: Was performed in subset of patients participating in the Main Study to assess the effect of the four randomised treatments on dynamic hyperinflation.

Extension Study: To establish whether the FEV1 time profile following combination bronchodilator therapy of tiotropium plus salmeterol is affected by the pharmaceutical formulation of salmeterol, i.e. the MDI or the Diskus®.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

97

Fase

  • Fase 2

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

40 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. All patients must sign an informed consent consistent with International Conference on Harmonization Good Clinical Practice (ICH-GCP) guidelines prior to participation in the trial, which includes medication washout and restrictions
  2. All patients must have a diagnosis of chronic obstructive pulmonary disease and must meet the following spirometric criteria:

    Patients must have relatively stable, moderate to severe airway obstruction with an FEV1 ≤ 60% of predicted normal and FEV1 ≤ 70% of FVC (Visits 1 and 2)

  3. Male or female patients 40 years of age or older
  4. Patients must be current or ex-smokers with a smoking history of more than 10 pack-years (Patients who had never smoked cigarettes have to be excluded)
  5. Patients must be able to perform technically acceptable pulmonary function tests and must be able to maintain records (Patient Daily Diary Card) during the study period as required in the protocol
  6. Patients must be able to inhale medication in a competent manner from the HandiHaler® device and from a metered dose inhaler (MDI)

Exclusion Criteria:

  1. Patients with significant diseases other than COPD will be excluded. A significant disease is defined as a disease which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study
  2. Patients with clinically relevant abnormal baseline haematology, blood chemistry, or urinalysis, if the abnormality defines a significant disease as defined in exclusion criterion No. 1
  3. Patients with a recent history (i.e. six months or less) of myocardial infarction
  4. Patients with any unstable or life-threatening cardiac arrhythmia or patients who have been hospitalised for such an event within the past year
  5. Patients with a malignancy for which the patient has undergone resection, Radiation therapy or chemotherapy within the last five years. Patients with treated basal cell carcinoma are allowed
  6. Patients with known narrow-angle glaucoma
  7. Patients with a history of asthma, allergic rhinitis or who have a total blood eosinophil count ≥600 mm3
  8. Patients with a history of life-threatening pulmonary obstruction, or a history of cystic fibrosis or clinically evident bronchiectasis
  9. Patients with known active tuberculosis
  10. Patients with a history of and/or active significant alcohol or drug abuse. See exclusion criterion No. 1
  11. Patients who have undergone thoracotomy with pulmonary resection. Patients with a history of thoracotomy for other reasons should be evaluated as per exclusion criterion No. 1
  12. Patients who have completed a pulmonary rehabilitation program in the six weeks prior to the Screening Visit (Visit 1)
  13. Patients who regularly use daytime oxygen therapy
  14. Patients who have taken an investigational drug within one month or six half lives (whichever is greater) prior to Screening Visit (Visit 1)
  15. Patients who are being treated with oral beta-adrenergics
  16. Patients who are being treated with cromolyn sodium or nedocromil sodium
  17. Patients who are being treated with antihistamines (H1 receptor antagonists), antileukotrienes or leukotriene receptor antagonists for asthma or excluded allergic conditions. See exclusion criterion No. 7
  18. Patients using oral corticosteroid medication at unstable doses (i.e., less than six weeks on a stable dose) or at doses in excess of the equivalent of 10 mg of prednisone per day or 20 mg every other day
  19. Patients with known hypersensitivity to anticholinergic drugs, beta-adrenergics, lactose or any other components of the medication delivery systems
  20. Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception for the previous 3 months (i.e. oral contraceptives, intrauterine devices, diaphragm or subdermal implants eg: Norplant®)
  21. Patients with previous participation (receipt of randomised treatment) in this study
  22. Patients who are currently participating in another study
  23. The randomisation of patients with any respiratory infection or COPD exacerbation in the six weeks prior to the Screening Visit (Visit 1) or during the baseline period should be postponed. Patients may be randomised six weeks following recovery from the infection or exacerbation

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Tiotropium+salmeterol QD
free combination of tiotropium and salmeterol
administered via HandiHaler®
administered via metered dose inhaler (MDI)
Comparatore attivo: Tiotropium+salmeterol BID
free combination of tiotropium and salmeterol
administered via HandiHaler®
administered via metered dose inhaler (MDI)
Comparatore attivo: Tiotropium QD
administered via HandiHaler®
Comparatore attivo: Salmeterol BID
administered via metered dose inhaler (MDI)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Area under the curve of forced expiratory volume in one second (FEV1 AUC0-24h)
Lasso di tempo: up to 12 hours after morning and evening dose
up to 12 hours after morning and evening dose
FEV1 AUC0-12h
Lasso di tempo: up to 12 hours after morning and evening dose
up to 12 hours after morning and evening dose

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of inhalations of rescue salbutamol therapy used per day
Lasso di tempo: weeks 4 to 6 of each treatment period
weeks 4 to 6 of each treatment period
FEV1 AUC12-24h
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
AUC of forced vital capacity (FVC AUC0-12h)
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
FVC AUC0-24h
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
FVC AUC12-24h
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
Peak FEV1
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
Trough FEV1
Lasso di tempo: after 6 weeks of each treatment
Trough FEV1 was defined as the pre-dose FEV1 measured just prior to the last administration of the morning dose of randomised treatment.
after 6 weeks of each treatment
Peak FVC
Lasso di tempo: after 6 weeks of each treatment
after 6 weeks of each treatment
Trough FVC
Lasso di tempo: after 6 weeks of each treatment
Trough FVC was defined as the pre-dose FVC measured just prior to the last administration of the morning dose of randomised treatment
after 6 weeks of each treatment
Individual FEV measurements at each time point
Lasso di tempo: up to 6 weeks
up to 6 weeks
Individual FVC measurements at each time point
Lasso di tempo: up to 6 weeks
up to 6 weeks
Peak expiratory flow rate (PEFR) measured twice daily
Lasso di tempo: weeks 4 to 6 of each treatment period
weeks 4 to 6 of each treatment period
Change in focal score of the Mahler Transition Dyspnea Index (TDI)
Lasso di tempo: after 6 weeks of each treatment
The TDI focal score is the sum of the three components of the TDI: Functional Impairment, Magnitude of Task and Magnitude of Effort
after 6 weeks of each treatment
Number of patients with adverse events
Lasso di tempo: up to 33 weeks
up to 33 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Collegamenti utili

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 settembre 2003

Completamento primario (Effettivo)

1 luglio 2004

Date di iscrizione allo studio

Primo inviato

16 settembre 2014

Primo inviato che soddisfa i criteri di controllo qualità

16 settembre 2014

Primo Inserito (Stima)

17 settembre 2014

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

17 settembre 2014

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 settembre 2014

Ultimo verificato

1 settembre 2014

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Placebo HandiHaler®

Sottoscrivi