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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UNKNOWN
200 participants
OBSERVATIONAL
2016-10-25
2023-12-31
Brief Summary
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The investigators decide to conduct a monocentric observational study to define the prevalence and characterization of cardiovascular comorbidities as well as markers of accelerated aging. We would like to test the hypothesis that cardiovascular comorbidities are frequent in bronchiectasis and may be associated with markers of inflammation and aging.
Phenotype of the lung disease will include: spirometry, plethysmography, DLCO measurement according to the ATS/ERS guideline. 6M walking test and echocardiography will be also performed.
Frequency of comorbidities will be calculated with data from questionnaire as well as standardized explorations.
Aging related manifestations will be measured: arterial stiffness using aortic pulse wave velocity, bone mineral density using dual energy X-ray absorptiometry. Appendicular skeletal muscle mass and grip test were also performed.
Blood test were also performed to measure inflammatory markers, cytokines and length of telomere in circulating leucocytes.
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Detailed Description
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Frequency of comorbidities will be calculated with data from questionnaire as well as standardized explorations.
Aging related manifestations will be measured: arterial stiffness using aortic pulse wave velocity, bone mineral density using dual energy X-ray absorptiometry. Appendicular skeletal muscle mass and grip test were also performed.
Blood test were also performed to measure inflammatory markers, cytokines and length of telomere in circulating leucocytes.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Formal diagnosis of bronchiectasis by imaging (CT-scan)
* For women, pregnancy test negative
* Affiliation to a social Security
* written inform consent
Exclusion Criteria
* Contre indication of one of the tests
* Exacerbation with hospitalization or outpatient clinic visit in the last 4 weeks.
* Unability to obtain an informed consent
* Pregnancy or Breast feeding
40 Years
80 Years
ALL
No
Sponsors
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Centre Hospitalier Intercommunal Creteil
OTHER
Responsible Party
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Bernard MAITRE
Pr
Principal Investigators
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Bernard MAITRE
Role: PRINCIPAL_INVESTIGATOR
CHI Créteil
Locations
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Chi Creteil
Créteil, , France
Countries
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Other Identifiers
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BRONCOCA
Identifier Type: -
Identifier Source: org_study_id
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