- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00686309
Comparison of On-line and Off-line Measurements of Exhaled Nitric Oxide (NO)
August 15, 2009 updated by: Ziv Hospital
Comparison of On-line and Off-line Measurements of Exhaled NO
Asthma is a major health problem worldwide.
The measurement of fractional exhaled nitric oxide (FENO) has been established as a valuable non invasive and simple tool in the diagnosis of asthma and may also act as a useful surrogate inflammatory marker on which to base treatment decisions in asthma management algorithms.
The measurement is useful also in other respiratory diseases.
Current methods of measuring FENO include on line measurements by heavy duty expensive analyzers which are not widely and easily available.
Off line measurements of breath samples which can be analysed later may be a simple solution.
We hypothesize tha toff line measurements of NO will be as reliable and valid as those measured on-line
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
200
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
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Safed, Israel
- Pediatric Department, Ziv Medical Center
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
General population bth healthy and with respiratory illness such as asthma, COPD, PCD, Rhinitis
Description
Inclusion Criteria:
- Volunteer to participate
- Filed a short health questionnaire
Exclusion Criteria:
- None
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
- Observational Models: Case-Crossover
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Off line measurement of exhaled NO
Time Frame: Two types of breathing in the same day
|
Two types of breathing in the same day
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
July 1, 2010
Primary Completion (Anticipated)
July 1, 2011
Study Completion (Anticipated)
July 1, 2011
Study Registration Dates
First Submitted
May 26, 2008
First Submitted That Met QC Criteria
May 28, 2008
First Posted (Estimate)
May 29, 2008
Study Record Updates
Last Update Posted (Estimate)
August 18, 2009
Last Update Submitted That Met QC Criteria
August 15, 2009
Last Verified
August 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HP8-295-R
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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