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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00798564
Other study ID # 34797
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2008
Est. completion date December 2009

Study information

Verified date March 2021
Source Skane University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The overall aim is to explore pathophysiological factors related to airway hyperresponsiveness to direct and indirect provocation stimuli in athletes with different sport activities, with special focus on epithelial reaction linked to CC16 and to eicosanoid related inflammatory response. The investigators also wish to compare indirect testing done as hyper osmotic challenge with Mannitol compared to a defined sport specific exercise challenge.


Description:

By non-invasive tools the investigators wish to characterize type of airway reaction to various provocative stimuli in athletes doing two different sort activities, Tennis or swimming. As controls are being used sedentary age-matched controls from the same region, exposed to the same school environment. Thus we wish to: - explore the prevalence of positive mannitol reactivity among swimmers and tennis player and how this relates to symptoms, disease history and to a sport specific exercise provocation test. - compare the results from sport specific testing with a standardized eucapnic hyperventilation test (EHV) - compare the overall reactivity to mannitol or EHV among swimmers and tennis players compared to aged matched controls. - explore the role by CC16 in airway reactivity to different provocative stimuli and to see whether there is a difference between different sport activities, different test protocols and between athletes and controls. - explore evidence of eicosanoid related inflammatory reaction in athletes and controls in relation to different provocative stimuli The study population consists of 100 elite swimmers, 100 elite tennis players and 100 non-elite, eged matched controls. In the latter group, 30 are aged matched non-atopic non-asthmatic controls.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date December 2009
Est. primary completion date July 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 25 Years
Eligibility Inclusion Criteria: - Subjects aged 16-19 from Skåne. - All should approve attendance in the study by signing an informed consent. Igf they are aged under 18, parents should also sign. - Three groups are included - Elite aspiring swimmers with an average training intensity of at least hours per week the last year. Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Skane University Hospital Swedish Heart Lung Foundation
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