Pressure Support Ventilation During CF Exacerbations
Primary Purpose
Cystic Fibrosis
Status
Suspended
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pressure support ventilation
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis
Eligibility Criteria
cystic fibrosis subjects with pulmonary exacerbation
Sites / Locations
- University of Minnesota
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00008775
First Posted
January 16, 2001
Last Updated
June 23, 2005
Sponsor
National Center for Research Resources (NCRR)
Collaborators
Cystic Fibrosis Foundation
1. Study Identification
Unique Protocol Identification Number
NCT00008775
Brief Title
Pressure Support Ventilation During CF Exacerbations
Official Title
Pressure Support Ventilation During CF Exacerbations: A Randomized, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2001
Overall Recruitment Status
Suspended
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
National Center for Research Resources (NCRR)
Collaborators
Cystic Fibrosis Foundation
4. Oversight
5. Study Description
Brief Summary
Chest physiotherapy is recognized as a mainstay of cystic fibrosis therapy, and is particularly important during treatment of pulmonary exacerbations. For some patients, especially those with moderate to severe compromise of lung function, this therapy may impose a high demand in the work of breathing and energy expenditure. The goal of this study is to evaluate the effectiveness of adding pressure support ventilation (PSV) during chest physiotherapy sessions in patients with cystic fibrosis with moderate to severe lung function compromise being treated for a pulmonary exacerbation.
Detailed Description
The proposed study will be conducted over three years. Cystic fibrosis patients with moderate to severe pulmonary disease who are experiencing an acute exacerbation that requires hospitalization will be admitted to the GCRC. Subject participation in the study will be for the first 10 days of hospitalization. Subjects will be randomized into one of two treatment groups: usual care or usual care plus non-invasive pressure support ventilation (PSV).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
None (Open Label)
Allocation
Randomized
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Pressure support ventilation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
cystic fibrosis subjects with pulmonary exacerbation
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Pressure Support Ventilation During CF Exacerbations
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