MedPath

Combivent Respimat 1-year Safety Study in Patients With Chronic Obstructive Pulmonary Disease

Phase 3
Completed
Conditions
Pulmonary Disease, Chronic Obstructive
Interventions
Registration Number
NCT01019694
Lead Sponsor
Boehringer Ingelheim
Brief Summary

The primary objective of this study is to evaluate long-term safety and patient acceptability of COMBIVENT RESPIMAT Inhalation Spray as compared to the COMBIVENT Inhalation Aerosol Chlorofluorocarbon-Metered Dose Inhaler (CFC-MDI) and the free combination of ATROVENT Hydrofluoroalkane (HFA) and albuterol Hydrofluoroalkane (HFA) inhalation aerosols.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
470
Inclusion Criteria

Not provided

Read More
Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Combivent Respimat 20/100 microgram(mcg)Combivent Respimat 20/100 mcgpatient to take 1 inhalation 4 times a day
Combivent CFC-MDI 36/206 microgram-mcgCombivent CFC-MDIpatient to take 2 inhalations 4 times a day
Atrovent HFA 42 mcg + Albuterol HFAAtrovent HFA 42 mcg + Albuterol HFA 200 mcgpatient to take 2 inhalations of each 4 times a day
Primary Outcome Measures
NameTimeMethod
Performance Domain Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 4848 weeks

Patient acceptability was assessed with the Performance Domain score from the PASAPQ. The score is a mean of 7 items on a scale from 0 (very dissatisfied) to 100 (very satisfied).

Secondary Outcome Measures
NameTimeMethod
Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 00 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 1212 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Performance Domain Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 33 weeks

Patient acceptability was assessed with the Performance Domain score from the PASAPQ. The score is a mean of 7 items on a scale from 0 (very dissatisfied) to 100 (very satisfied).

Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 2424 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 3636 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 4848 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 00 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 33 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 1212 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 2424 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 3636 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Clinical COPD Questionnaire (CCQ) Symptom Domain Score at Week 4848 weeks

CCQ symptom domain score assessed patient feelings or limitations due to their COPD on a scale from 0 (not limited) to 6 (totally limited).

Physician's Global Evaluation at Week 00 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Physician's Global Evaluation at Week 33 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Physician's Global Evaluation at Week 1212 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Physician's Global Evaluation at Week 2424 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Physician's Global Evaluation at Week 3636 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Physician's Global Evaluation at Week 4848 weeks

Physicians evaluated the patient's overall clinical condition on a scale ranging from "poor" (score 1 or 2) to "excellent" (score 7 or 8).

Change From Baseline in FEV1 at Day 1baseline, day 1

Change from test-day baseline in Forced Expiratory Volume in 1 second (FEV1) at 1 hour post dose on test day 1.

Change From Baseline in FEV1 at Week 12baseline, 12 weeks

Change from test-day baseline in Forced Expiratory Volume in 1 second (FEV1) at 1 hour post dose at Week 12

Change From Baseline in FEV1 at Week 24baseline, 24 weeks

Change from test-day baseline in Forced Expiratory Volume in 1 second (FEV1) at 1 hour post dose at Week 24

Overall Satisfaction Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 33 weeks

Patient satisfaction was assessed by asking: "Overall, how satisfied are you with your inhaler?". Responses were made on a scale from 1 (very dissatisfied) to 7 (very satisfied).

Performance Domain Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 1212 weeks

Patient acceptability was assessed with the Performance Domain score from the PASAPQ. The score is a mean of 7 items on a scale from 0 (very dissatisfied) to 100 (very satisfied).

Performance Domain Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 2424 weeks

Patient acceptability was assessed with the Performance Domain score from the PASAPQ. The score is a mean of 7 items on a scale from 0 (very dissatisfied) to 100 (very satisfied).

Performance Domain Score From the Patient Satisfaction and Preference Questionnaire (PASAPQ) at Week 3636 weeks

Patient acceptability was assessed with the Performance Domain score from the PASAPQ. The score is a mean of 7 items on a scale from 0 (very dissatisfied) to 100 (very satisfied).

Change From Baseline in FEV1 at Week 48baseline, 48 weeks

Change from test-day baseline in Forced Expiratory Volume in 1 second (FEV1) at 1 hour post dose at Week 48

Change From Baseline in FVC at Day 1baseline, day 1

Change from test-day baseline in Forced Vital Capacity (FVC) at 1 hour post dose on test day 1.

Change From Baseline in FVC at Week 12baseline, 12 weeks

Change from test-day baseline in Forced Vital Capacity (FVC) at 1 hour post dose at Week 12

Change From Baseline in FVC at Week 24baseline, 24 weeks

Change from test-day baseline in Forced Vital Capacity (FVC) at 1 hour post dose at Week 24

Change From Baseline in FVC at Week 48baseline, 48 weeks

Change from test-day baseline in Forced Vital Capacity (FVC) at 1 hour post dose at Week 48

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 00 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 0

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 33 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 3

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 1212 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 12

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 2424 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 24

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 3636 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 36

Mean Number of Puffs of Daily Rescue Medication Use in Two Weeks Prior to Week 4848 weeks

Mean number of puffs of daily rescue medication use (albuterol use per 24 hour period) in two weeks prior to week 48

Number of Patients Having Chronic Obstructive Pulmonary Disease (COPD) Exacerbations48 weeks
Number of Patients Having Chronic Obstructive Pulmonary Disease (COPD) Exacerbations Leading to Hospitalization48 weeks

Trial Locations

Locations (55)

1012.62.117 Boehringer Ingelheim Investigational Site

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Livonia, Michigan, United States

1012.62.126 Boehringer Ingelheim Investigational Site

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Fort Collins, Colorado, United States

1012.62.123 Boehringer Ingelheim Investigational Site

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Waterbury, Connecticut, United States

1012.62.131 Boehringer Ingelheim Investigational Site

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Wheat Ridge, Colorado, United States

1012.62.116 Boehringer Ingelheim Investigational Site

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Lafayette, Louisiana, United States

1012.62.155 Boehringer Ingelheim Investigational Site

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Boulder, Colorado, United States

1012.62.113 Boehringer Ingelheim Investigational Site

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Coeur d'Alene, Idaho, United States

1012.62.109 Boehringer Ingelheim Investigational Site

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Greer, South Carolina, United States

1012.62.122 Boehringer Ingelheim Investigational Site

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Danville, Virginia, United States

1012.62.152 Boehringer Ingelheim Investigational Site

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Killeen, Texas, United States

1012.62.108 Boehringer Ingelheim Investigational Site

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Spokane, Washington, United States

1012.62.133 Boehringer Ingelheim Investigational Site

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Spokane, Washington, United States

1012.62.156 Boehringer Ingelheim Investigational Site

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Mesa, Arizona, United States

1012.62.141 Boehringer Ingelheim Investigational Site

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Riverside, California, United States

1012.62.144 Boehringer Ingelheim Investigational Site

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Stamford, Connecticut, United States

1012.62.114 Boehringer Ingelheim Investigational Site

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Clearwater, Florida, United States

1012.62.130 Boehringer Ingelheim Investigational Site

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Easley, South Carolina, United States

1012.62.118 Boehringer Ingelheim Investigational Site

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Spartanburg, South Carolina, United States

1012.62.146 Boehringer Ingelheim Investigational Site

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Decatur, Georgia, United States

1012.62.101 Boehringer Ingelheim Investigational Site

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Morgantown, West Virginia, United States

1012.62.143 Boehringer Ingelheim Investigational Site

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Houston, Texas, United States

1012.62.107 Boehringer Ingelheim Investigational Site

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Cincinnati, Ohio, United States

1012.62.102 Boehringer Ingelheim Investigational Site

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San Antonio, Texas, United States

1012.62.129 Boehringer Ingelheim Investigational Site

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St. Louis, Missouri, United States

1012.62.139 Boehringer Ingelheim Investigational Site

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Pensacola, Florida, United States

1012.62.145 Boehringer Ingelheim Investigational Site

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Mobile, Alabama, United States

1012.62.153 Boehringer Ingelheim Investigational Site

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Jasper, Alabama, United States

1012.62.135 Boehringer Ingelheim Investigational Site

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Berkeley, California, United States

1012.62.112 Boehringer Ingelheim Investigational Site

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Albuquerque, New Mexico, United States

1012.62.137 Boehringer Ingelheim Investigational Site

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North Dartmouth, Massachusetts, United States

1012.62.111 Boehringer Ingelheim Investigational Site

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Rochester, New York, United States

1012.62.150 Boehringer Ingelheim Investigational Site

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Toledo, Ohio, United States

1012.62.157 Boehringer Ingelheim Investigational Site

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Dubuque, Iowa, United States

1012.62.103 Boehringer Ingelheim Investigational Site

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Philadelphia, Pennsylvania, United States

1012.62.124 Boehringer Ingelheim Investigational Site

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Deland, Florida, United States

1012.62.115 Boehringer Ingelheim Investigational Site

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Winter Park, Florida, United States

1012.62.127 Boehringer Ingelheim Investigational Site

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St. Louis, Missouri, United States

1012.62.147 Boehringer Ingelheim Investigational Site

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Cherry Hill, New Jersey, United States

1012.62.149 Boehringer Ingelheim Investigational Site

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Summit, New Jersey, United States

1012.62.161 Boehringer Ingelheim Investigational Site

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Greenville, South Carolina, United States

1012.62.154 Boehringer Ingelheim Investigational Site

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East Providence, Rhode Island, United States

1012.62.104 Boehringer Ingelheim Investigational Site

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Pittsburgh, Pennsylvania, United States

1012.62.158 Boehringer Ingelheim Investigational Site

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Minneapolis, Minnesota, United States

1012.62.120 Boehringer Ingelheim Investigational Site

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Cincinnati, Ohio, United States

1012.62.140 Boehringer Ingelheim Investigational Site

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Fort Worth, Texas, United States

1012.62.105 Boehringer Ingelheim Investigational Site

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Tacoma, Washington, United States

1012.62.151 Boehringer Ingelheim Investigational Site

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Greenville, South Carolina, United States

1012.62.134 Boehringer Ingelheim Investigational Site

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Tampa, Florida, United States

1012.62.132 Boehringer Ingelheim Investigational Site

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Ann Arbor, Michigan, United States

1012.62.159 Boehringer Ingelheim Investigational Site

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Louisville, Kentucky, United States

1012.62.148 Boehringer Ingelheim Investigational Site

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New Orleans, Louisiana, United States

1012.62.128 Boehringer Ingelheim Investigational Site

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Charleston, South Carolina, United States

1012.62.119 Boehringer Ingelheim Investigational Site

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Richmond, Virginia, United States

1012.62.142 Boehringer Ingelheim Investigational Site

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Richmond, Virginia, United States

1012.62.125 Boehringer Ingelheim Investigational Site

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Austin, Texas, United States

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