- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01403467
Impact of Continuous Positive Airway Pressure on the Treatment of Acute Asthma Exacerbation
July 26, 2011 updated by: Ramathibodi Hospital
This current study aimed to demonstrate the effectiveness of the addition of CPAP to the current conventional therapy in terms of airway obstruction improvement in acute asthma patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Continuous positive airway pressure (CPAP) is widely used in providing ventilator support.
However, its role in an acute asthmatic attack is uncertain.
The purpose of this study was to compare the efficacy of CPAP when used in addition to conventional therapy with conventional therapy alone in the management of acute asthma exacerbation.
Study Type
Interventional
Enrollment (Actual)
86
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bangkok, Thailand, 10400
- Ramathibodi hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged over 18 years
- known asthmatic patients visiting ED with acute exacerbation
- had given their written informed consent.
Exclusion Criteria:
- smoking history
- chronic obstructive pulmonary disease
- required intubation
- instability of hemodynamic or arrhythmia
- unable to perform PEFR
- facial abnormality
- pulmonary infiltration
- pregnancy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: NIPPV
|
CPAP 8 cmH2O
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
an improvement in PEFR, as % predicted
Time Frame: 75 mins
|
75 mins
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yuda Sutherasan, M.D., Ramathibodi Hospital, Mahidol University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2009
Primary Completion (Actual)
January 1, 2010
Study Completion (Actual)
January 1, 2011
Study Registration Dates
First Submitted
July 25, 2011
First Submitted That Met QC Criteria
July 26, 2011
First Posted (Estimate)
July 27, 2011
Study Record Updates
Last Update Posted (Estimate)
July 27, 2011
Last Update Submitted That Met QC Criteria
July 26, 2011
Last Verified
December 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 02-52-28
- MURA2009/1239 (Other Identifier: Ramathibodi Hospital)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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