Clinical Study of Intermittent Positive Pressure Breathing (IPPB)
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Accession Number
HLB00090013a
Study Type
Clinical Trial
Collection Type
Open BioLINCC Study
See bottom of this webpage for request information
Study Period
1976-1983
NHLBI Division
DLD
Dataset(s) Last Updated
January 3, 2018
Clinical Trial URLs
https://clinicaltrials.gov/ct/show/NCT00000565
Primary Publication URLs
N/A
Consent
Commercial Use Data Restrictions No
Data Restrictions Based On Area Of Research No
Objectives
To evaluate the efficacy of long-term intermittent positive pressure breathing (IPPB) treatment when used as an adjunct to the overall care of ambulatory outpatients with chronic obstructive pulmonary disease. The evaluation compared the use of IPPB with use of a powered nebulizer.
Design
Multicenter randomized controlled clinical trial. Criteria for inclusion: Men and women, ages 30 to 74, who were ambulatory and had symptomatic chronic bronchitis or emphysema.
Conclusions
Compliance with treatment, lung function, and quality of life were evaluated at regular intervals during follow-up, and records were kept of hospitalizations and vital status. Treatment compliance was less than optimal; only half of the patients used their devices for the prescribed amount of time or 10 minutes at least three times a day. Although this was disappointing, it was probably the best compliance that could be attained. There was no statistically significant difference between the treatment groups in mortality, rate and duration of hospitalizations, or change in lung function or life quality with time, overall or for clinically relevant subgroups. The trial group saw no advantage of IPPB over compressor nebulizer therapy and concluded that, if an advantage existed, it must be marginal.
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Resources Available
Study Datasets OnlyStudy Documents
- Data Dictionary (PDF - 764.8 KB)
- Manual of Procedures (PDF - 8.7 MB)
- Protocol for Collaborative Program (PDF - 3.2 MB)
- Protocol for Neuropsychological and Quality of Life Measures (PDF - 1.6 MB)
- Forms
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