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Measure of the Long Term Influence of SPIRIVA® in Acute Respiratory Disorders

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Tiotropium
Sponsored by
Boehringer Ingelheim
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive

Eligibility Criteria

41 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Diagnosis of COPD according to the European Respiratory Society (ERS) (R95-3225) and matching the following criteria: Stable moderate to severe airway obstruction Baseline 30 % < FEV1 < 65 % of European Community of Coal and Steel (ECCS) predicted values (R94-1408). Baseline FEV1/SVC< 70 %. Smoking history > 10 pack-years (p.y.). A p.y. was defined as the equivalent of smoking One pack of cigarettes per day for one year. History of exacerbation in the past year.

Sites / Locations

  • Clinique Saint Sauveur
  • Boehringer Ingelheim Investigational Site
  • Clinique la Casamance
  • Boehringer Ingelheim Investigational Site
  • Hôpital
  • GPL
  • CH Cholet
  • Boehringer Ingelheim Investigational Site
  • Boehringer Ingelheim Investigational Site
  • Hôpital Gabriel Montpied
  • Clinique des Cèdres
  • Clinique Saint Vincent
  • Centre Hospitalier Auban Moet
  • Boehringer Ingelheim Investigational Site
  • Boehringer Ingelheim Investigational Site
  • Hôpital Calmette
  • Boehringer Ingelheim Investigational Site
  • Boehringer Ingelheim Investigational Site
  • CH Lyon Sud
  • Hôpital de la Croix-Rousse
  • Hôpital Louis Pradel
  • Hôpital Louis Pradel
  • Boehringer Ingelheim Investigational Site
  • Hôpital Ambroise Paré
  • Hôpital Nord
  • CHG
  • Boehringer Ingelheim Investigational Site
  • Hôpital N.D. bon Secours
  • Centre Hospitalier Universitaire Arnaud de Villeneuve
  • Service des maladies respiratoires
  • Polyclinique Les Fleurs
  • Fondation Saint Joseph
  • Hôpital Cochin
  • Hôpital Bichat-Claude Bernard
  • Hôpital Tenon
  • Hôpital Hôtel Dieu
  • Hôpital St Antoine
  • CTAR
  • Groupe Médical Saint Rémi
  • Hôpital Charles Nicolle
  • CHILTERN
  • CHD Félix Guyon
  • Nouvelle Clinique Union et Vaurais
  • Centre Hospitalier Sud-Réunion
  • Boehringer Ingelheim Investigational Site
  • Boehringer Ingelheim Investigational Site
  • Boehringer Ingelheim Investigational Site
  • Hôpital Hautepierre
  • Boehringer Ingelheim Investigational Site
  • CHU Purpan
  • Cabinet de Pneumologie
  • Cabinet Médical
  • Clinique Saint Jean Lanquedoc
  • CHU Rangueil
  • Centre Hospitalier

Outcomes

Primary Outcome Measures

morning peak expiratory flow rate (PEFR)

Secondary Outcome Measures

incidence, severity and duration of exacerbations
number of patients with one or more exacerbation
rate of PEFR drops
number of lost working days
number of days of hospitalisation
use of rescue medications, type and duration
bacterial and viral characterisation of severe exacerbations
spirometric evaluation (FEV1, FVC, SVC, MEF25-75 ) and optional measurements (IC)
plethysmography (RV, TLC) (optional)
Adverse events, physical examination

Full Information

First Posted
January 9, 2006
Last Updated
October 31, 2013
Sponsor
Boehringer Ingelheim
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1. Study Identification

Unique Protocol Identification Number
NCT00274014
Brief Title
Measure of the Long Term Influence of SPIRIVA® in Acute Respiratory Disorders
Official Title
Effects of Inhaled Tiotropium Bromide on Severity of Airflow Obstruction During Long-term Treatment in Patients With Moderately Severe Copd. Impact on Severity and Incidence of Exacerbations.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
October 2000 (undefined)
Primary Completion Date
October 2003 (Actual)
Study Completion Date
October 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Boehringer Ingelheim

4. Oversight

5. Study Description

Brief Summary
The objectives of this study were to evaluate the effect of a one-year treatment with inhaled tiotropium bromide 18 mcg once daily on lung function, incidence and severity of exacerbations in patients with chronic obstructive pulmonary disease (COPD). The secondary purpose was to explore possible relationships between lung function changes and occurrence of COPD exacerbations and to try to characterize these exacerbations.
Detailed Description
This was a multicentre, randomised, double blind, parallel group, placebo-controlled, one year study. It was designed to determine the effect of inhaled tiotropium treatment on airflow obstruction (PEFR), incidence and severity of exacerbations in patients with COPD. Following an initial 3-week screening period qualifying patients were randomized to either tiotropium or placebo at Visit 2. Patients returned to the clinic at weeks 6 (Visit 3), 12 (Visit 4), 24 (Visit 5), 36 (Visit 6), 48 (Visit 7) and at Week 50 for the conclusion of the trial (Visit 8). The patients received treatment daily for 48 weeks (336 days). PEFR, as well as use of rescue medication and respiratory condition, were self-assessed by patients and recorded every morning on a graphical diary card every morning. The graphical presentation of these data was supposed to help investigators to detect exacerbations occurring between two consecutive visits. Details on hospitalizations due to COPD exacerbations were recorded in a special hospitalization booklet. Study Hypothesis: The objectives of this study were to evaluate the effect of a one-year treatment with inhaled tiotropium bromide 18 mcg once daily on lung function, incidence and severity of exacerbations in patients with chronic obstructive pulmonary disease (COPD). The secondary purpose was to explore possible relationships between lung function changes and occurrence of COPD exacerbations and to try to characterize these exacerbations. Comparison(s): Tiotropium 18 mcg once daily vs Placebo

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
1000 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Tiotropium
Primary Outcome Measure Information:
Title
morning peak expiratory flow rate (PEFR)
Time Frame
50 weeks
Secondary Outcome Measure Information:
Title
incidence, severity and duration of exacerbations
Time Frame
50 weeks
Title
number of patients with one or more exacerbation
Time Frame
50 weeks
Title
rate of PEFR drops
Time Frame
50 weeks
Title
number of lost working days
Time Frame
50 weeks
Title
number of days of hospitalisation
Time Frame
50 weeks
Title
use of rescue medications, type and duration
Time Frame
50 weeks
Title
bacterial and viral characterisation of severe exacerbations
Time Frame
50 weeks
Title
spirometric evaluation (FEV1, FVC, SVC, MEF25-75 ) and optional measurements (IC)
Time Frame
50 weeks
Title
plethysmography (RV, TLC) (optional)
Time Frame
50 weeks
Title
Adverse events, physical examination
Time Frame
50 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Diagnosis of COPD according to the European Respiratory Society (ERS) (R95-3225) and matching the following criteria: Stable moderate to severe airway obstruction Baseline 30 % < FEV1 < 65 % of European Community of Coal and Steel (ECCS) predicted values (R94-1408). Baseline FEV1/SVC< 70 %. Smoking history > 10 pack-years (p.y.). A p.y. was defined as the equivalent of smoking One pack of cigarettes per day for one year. History of exacerbation in the past year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Boehringer Ingelheim Study Coordinator
Organizational Affiliation
BI France S.A.S.
Official's Role
Study Chair
Facility Information:
Facility Name
Clinique Saint Sauveur
City
Angers
ZIP/Postal Code
49000
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Annecy
ZIP/Postal Code
74000
Country
France
Facility Name
Clinique la Casamance
City
Aubagne
ZIP/Postal Code
13675
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Avrille
ZIP/Postal Code
49240
Country
France
Facility Name
Hôpital
City
Bois Guillaume cedex
ZIP/Postal Code
76233
Country
France
Facility Name
GPL
City
Caluire
ZIP/Postal Code
69300
Country
France
Facility Name
CH Cholet
City
Cholet
ZIP/Postal Code
49235
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Cholet
ZIP/Postal Code
49300
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Châlons en Champagne
ZIP/Postal Code
51000
Country
France
Facility Name
Hôpital Gabriel Montpied
City
Clermont-Ferrand cedex 1
ZIP/Postal Code
63003
Country
France
Facility Name
Clinique des Cèdres
City
Cornebarrieu
ZIP/Postal Code
31700
Country
France
Facility Name
Clinique Saint Vincent
City
Epernay
ZIP/Postal Code
51200
Country
France
Facility Name
Centre Hospitalier Auban Moet
City
Epernay
ZIP/Postal Code
51201
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Le Blanc Mesnil cedex
ZIP/Postal Code
93156
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Le petit Quevilly
ZIP/Postal Code
76140
Country
France
Facility Name
Hôpital Calmette
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Lyon
ZIP/Postal Code
69003
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Lyon
ZIP/Postal Code
69008
Country
France
Facility Name
CH Lyon Sud
City
Lyon
ZIP/Postal Code
69310
Country
France
Facility Name
Hôpital de la Croix-Rousse
City
Lyon
ZIP/Postal Code
69317
Country
France
Facility Name
Hôpital Louis Pradel
City
Lyon
ZIP/Postal Code
69394
Country
France
Facility Name
Hôpital Louis Pradel
City
Lyon
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Marseille
ZIP/Postal Code
13006
Country
France
Facility Name
Hôpital Ambroise Paré
City
Marseille
ZIP/Postal Code
13006
Country
France
Facility Name
Hôpital Nord
City
Marseille
ZIP/Postal Code
13015
Country
France
Facility Name
CHG
City
Martigues
ZIP/Postal Code
13500
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Metz
ZIP/Postal Code
57000
Country
France
Facility Name
Hôpital N.D. bon Secours
City
Metz
ZIP/Postal Code
57038
Country
France
Facility Name
Centre Hospitalier Universitaire Arnaud de Villeneuve
City
Montpellier Cedex 5
ZIP/Postal Code
34295
Country
France
Facility Name
Service des maladies respiratoires
City
Montpellier
ZIP/Postal Code
34000
Country
France
Facility Name
Polyclinique Les Fleurs
City
Ollioules
ZIP/Postal Code
83192
Country
France
Facility Name
Fondation Saint Joseph
City
Paris cedex 14
ZIP/Postal Code
75674
Country
France
Facility Name
Hôpital Cochin
City
Paris cedex 14
ZIP/Postal Code
75679
Country
France
Facility Name
Hôpital Bichat-Claude Bernard
City
Paris cedex 18
ZIP/Postal Code
75877
Country
France
Facility Name
Hôpital Tenon
City
Paris cedex 20
ZIP/Postal Code
75970
Country
France
Facility Name
Hôpital Hôtel Dieu
City
Paris
ZIP/Postal Code
75004
Country
France
Facility Name
Hôpital St Antoine
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
CTAR
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Groupe Médical Saint Rémi
City
Reims
ZIP/Postal Code
51100
Country
France
Facility Name
Hôpital Charles Nicolle
City
Rouen cedex
ZIP/Postal Code
76031
Country
France
Facility Name
CHILTERN
City
Rueil Malmaison cedex
ZIP/Postal Code
92508
Country
France
Facility Name
CHD Félix Guyon
City
Saint Denis de la Réunion
ZIP/Postal Code
97405
Country
France
Facility Name
Nouvelle Clinique Union et Vaurais
City
Saint Jean
ZIP/Postal Code
31240
Country
France
Facility Name
Centre Hospitalier Sud-Réunion
City
Saint-Pierre Cedex
ZIP/Postal Code
97448
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Salon de Provence
ZIP/Postal Code
13300
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Saumur
ZIP/Postal Code
49400
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Strasbourg
ZIP/Postal Code
67000
Country
France
Facility Name
Hôpital Hautepierre
City
Strasbourg
ZIP/Postal Code
67098
Country
France
Facility Name
Boehringer Ingelheim Investigational Site
City
Sélestat
ZIP/Postal Code
67600
Country
France
Facility Name
CHU Purpan
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
Cabinet de Pneumologie
City
Toulouse
ZIP/Postal Code
31076
Country
France
Facility Name
Cabinet Médical
City
Toulouse
ZIP/Postal Code
31300
Country
France
Facility Name
Clinique Saint Jean Lanquedoc
City
Toulouse
ZIP/Postal Code
31400
Country
France
Facility Name
CHU Rangueil
City
Toulouse
ZIP/Postal Code
31403
Country
France
Facility Name
Centre Hospitalier
City
Villefranche Sur Saône
ZIP/Postal Code
69655
Country
France

12. IPD Sharing Statement

Links:
URL
http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.214.pdf
Description
Related Info
URL
http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.214_literature.pdf
Description
Related Info

Learn more about this trial

Measure of the Long Term Influence of SPIRIVA® in Acute Respiratory Disorders

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