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OpenTrials
Completed

NCT Number: NCT01197690

Association Between Fractional Exhaled Nitric Oxide and Asthma Control

The purpose of this study is to determine mean or median of fractional exhaled nitric oxide (FeNO) in Thai atopic asthmatic patients that divided into subgroups due to level of asthma control according to the global initiative for asthma guideline.

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Key information

Age range

7 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Siriraj Hospital

Bangkok, Thailand

About this study

From many previous studies, fractional exhaled nitric oxide (FeNO) has many benefits such as non-invasive, easily to perform, less time consume, has direct association with severity of inflammation of bronchial trees and sputum eosinophils, has benefit for diagnosis and monitoring the treatment in asthmatic patients.

In Thailand, this field of study is less extend, especially in children population. We hypothesized that in uncontrolled or partly controlled group may have high level of fractional exhaled nitric oxide (FeNO) than controlled group.

It is therefore desirable to examine the association between fractional exhaled nitric oxide (FeNO) and level of asthma control among atopic asthmatic Thai children and will be the main objective of this research.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinical diagnosis of atopic bronchial asthma
  • follow up in clinic of allergy and clinical immunology, Siriraj hospital

Exclusion criteria

  • smoker or past history of smoking
  • has chronic disease eg. HIV infection, pulmonary hypertension, systemic lupus erythematosus, liver cirrhosis, gastroesophageal reflux, COPD, bronchiectasis
  • drink ethanol within 48 hours before enrollment
  • history of upper or lower respiratory tract infection within 6 weeks before enrollment
  • drink caffeine within day before enrollment
  • during pregnancy
  • history of systemic steroid use within 8 weeks before enrollment

Treatment and study plan

Primary outcomes

  1. fractional exhaled nitric oxide level

    Time frame: 10 minutes (average time), on the day of enrollment

Secondary outcomes

  1. scores of asthma control test: ACT

    Time frame: 5 minutes (average time), on the day of enrollment

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Acronym: FeNO_AS

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Sep 9, 2010
Registry last updated
Sep 18, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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