Study of the Physiology of the Asthma of the Obese Subjects. Breathing Obesity Asthma Study (BOA)
NCT ID: NCT00577733
Last Updated: 2013-09-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
204 participants
OBSERVATIONAL
2008-01-31
2010-11-30
Brief Summary
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Detailed Description
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Aims: The aim of this study is to evaluate whether 1) the variability of their diurnal ventilation (based on the measurement of CVTV and FDI) in three groups of women: obese with AHR, obese without AHR and healthy non obese (main objective), 2) obesity-related asthma pathophysiology is linked to atopy, and 3) obese asthmatic women have a greater decrease in ventilation variability as compared to non asthmatic obese women (secondary objectives).
Methods: The prevalence of AHR and confirmed asthma (international clinical and functional definition) are determined based on pulmonary function test (spirometry, volume determinations, arterial blood gas, measurement of the resistance of the respiratory system with evaluation of the response to deep inhalation, methacholine challenge, exhaled NO measurement, nocturnal polygraphy and oeso-gastroscopy) results obtained from 150 obese (BMI \> 35). The FDI and CVTV will be determined based on the tidal volume obtained from thoracic and abdominal plethysmography inductance measurements during the polygraphy. A nocturnal polygraphy is systematically done in these women to search for a Sleep Apnea Syndrome. 30 healthy (non asthmatic, normal exhaled NO value, BMI 18.5 to 25) women will constitute a control group. The size of the groups have been calculated based on literature data concerning the FDI and CVTV.
Analysis criteria: The prevalences of asthma (or asthma-like symptoms) and AHR will be of 30% and 50% (based on a personal preliminary study), respectively. The FDI and CVTV will be compared in obese women with and without AHR and in healthy women (primary objective), and subsequently in obese asthmatic women and obese non asthmatic women. The measurement of exhaled NO and the bronchomotor effect of deep inhalation will allow the determination of underlying pathophysiology of obesity-related asthma (secondary objective).
Perspectives: If our hypothesis is verified, obesity treatment will become part of the management of asthma in women.
Conditions
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Keywords
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Study Design
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PROSPECTIVE
Study Groups
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obese
obese
No interventions assigned to this group
healthy volunteers
healthy volunteers
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* age\>18 and \< 55 years
* BMI\>35 (\< 25 for healthy women)
* planned bariatric surgery
Exclusion Criteria
* pregnant or breast-feeding women
* No affiliation or non beneficiary of the National Health Insurance
18 Years
55 Years
FEMALE
Yes
Sponsors
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Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
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Principal Investigators
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DELCLAUX MD Christophe, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Physiology, Hôpital Européen Georges Pompidou
Locations
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Department of Physiology, Hôpital Européen Georges Pompidou
Paris, , France
Countries
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Other Identifiers
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P061010
Identifier Type: -
Identifier Source: org_study_id