Cardiorespiratory Performance and Pulmonary Microbiome in Patients After Repair of Esophageal Atresia
NCT ID: NCT03767673
Last Updated: 2018-12-06
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
NA
50 participants
INTERVENTIONAL
2017-08-10
2019-09-02
Brief Summary
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The aim of this prospective study is to investigate the cardiopulmonary performance capacity and the pulmonary microbiome of adolescent and adult patients with corrected esophageal atresia and to compare the results with a control group. Another focus of the investigators is on the composition of the pulmonary microbiome of the participants. Changes of the pulmonary microbiome and the influence on the cardio-pulmonary performance capacity have not yet been investigated. Furthermore, it should be investigated whether the treatment measures and a complicated disease course in the neonatal period have long-term effects on lung function, exercise capacity and composition of the microbiome in the lungs.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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Patients after esophageal atresia
Patients older than 12 years following surgical repair of congenital esophageal atresia will be included after written informed consent. Patients will be subjected to spirometry to determine their age, weight (determined by Kilogram (kg) on a medical weight scale) and Vital Capacity before (initial Spirometry) and after (final Spirometry) exercise performance testing. Bicycle ergospirometer will be applied to determine the Maximum Oxygen Uptake and the Maximum Performance. Thereafter deep induced sputum will be harvested for measurements of the pulmonary microbiome (Pulmonary Microbiome 16S rDNA profiling).
Pulmonary microbiome (16S rDNA profiling)
Harvesting of deep induced sputum and determination of the airway microbiome by 16S ribosomal RNA (rRNA) pyrosequencing. Evaluation of alpha and beta diversity and relative bacterial abundance at the genus level. Measurements will be performed in both groups (samples will be harvested within 30 minutes after spiroergometry).
Maximum oxygen uptake
Determination of the maximum oxygen uptake (ml/kg/min) corrected for gender, age and body weight by bicycle spiroergometry. Measurements will be performed in both groups.
Maximum performance
Determination of the maximum performance (W/kg) corrected for body weight by bicycle spiroergometry. Measurements will be performed in both groups.
weight
Determined by Kilogram on a medical weight scale
age
Determination of age by patient's Report and past medical history
Initial Spirometry
Determination of Vital Capacity by spirometry before (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Final Spirometry
Determination of Vital Capacity by spirometry after (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Control group
Age and sex matched adolescents will be recruited as control group and will be included after written informed consent. Adolescents will be subjected to spirometry to determine their age, weight (determined by Kilogram on a medical weight scale) and Vital Capacity before (initial Spirometry) and after (final Spirometry) exercise performance testing. Bicycle ergospirometer will be applied to determine the Maximum Oxygen Uptake and the Maximum Performance. Thereafter deep induced sputum will be harvested for measurements of the pulmonary microbiome (Pulmonary Microbiome 16S rDNA profiling).
Pulmonary microbiome (16S rDNA profiling)
Harvesting of deep induced sputum and determination of the airway microbiome by 16S ribosomal RNA (rRNA) pyrosequencing. Evaluation of alpha and beta diversity and relative bacterial abundance at the genus level. Measurements will be performed in both groups (samples will be harvested within 30 minutes after spiroergometry).
Maximum oxygen uptake
Determination of the maximum oxygen uptake (ml/kg/min) corrected for gender, age and body weight by bicycle spiroergometry. Measurements will be performed in both groups.
Maximum performance
Determination of the maximum performance (W/kg) corrected for body weight by bicycle spiroergometry. Measurements will be performed in both groups.
weight
Determined by Kilogram on a medical weight scale
age
Determination of age by patient's Report and past medical history
Initial Spirometry
Determination of Vital Capacity by spirometry before (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Final Spirometry
Determination of Vital Capacity by spirometry after (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Interventions
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Pulmonary microbiome (16S rDNA profiling)
Harvesting of deep induced sputum and determination of the airway microbiome by 16S ribosomal RNA (rRNA) pyrosequencing. Evaluation of alpha and beta diversity and relative bacterial abundance at the genus level. Measurements will be performed in both groups (samples will be harvested within 30 minutes after spiroergometry).
Maximum oxygen uptake
Determination of the maximum oxygen uptake (ml/kg/min) corrected for gender, age and body weight by bicycle spiroergometry. Measurements will be performed in both groups.
Maximum performance
Determination of the maximum performance (W/kg) corrected for body weight by bicycle spiroergometry. Measurements will be performed in both groups.
weight
Determined by Kilogram on a medical weight scale
age
Determination of age by patient's Report and past medical history
Initial Spirometry
Determination of Vital Capacity by spirometry before (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Final Spirometry
Determination of Vital Capacity by spirometry after (within 30 minutes) spiroergometry. Measurements will be performed in both groups.
Eligibility Criteria
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Inclusion Criteria
* Status post surgical correction of esophageal atresia with and without fistula
* Granted consent
Exclusion Criteria
* Other associated serious malformations
* Acute, temporary respiratory complaints (cough, allergies etc.)
* Physical and mental illnesses or disabilities that do not allow the examination to be carried out
* non-granted consent
12 Years
ALL
Yes
Sponsors
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Medical University of Graz
OTHER
Responsible Party
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Principal Investigators
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Jana Windhaber, MD
Role: STUDY_DIRECTOR
Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria
Holger Till, MD
Role: STUDY_CHAIR
Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria
Christoph Arneitz, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria
Locations
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Medical University of Graz
Graz, , Austria
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1.1
Identifier Type: -
Identifier Source: org_study_id
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