Cardiorespiratory Performance and Pulmonary Microbiome in Patients After Repair of Esophageal Atresia

NCT03767673 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-12-06

No results posted yet for this study

Summary

The majority of the clinical research on esophageal atresia focuses on the upper gastrointestinal tract. However, the trachea and the lung are also affected in many of these children, so that a lifelong pulmonary impairment may result. The importance of respiratory function in the context of follow-up of these patients has therefore been increasingly recognized in recent years. Scientific work has shown significantly, that patients following esophageal atresia repair develop respiratory symptoms more frequently than the normal population. Mild impairment of the pulmonary function in adolescence and adulthood was demonstrated in some studies, but to date, there is no exact idea about the relationship between early childhood disease progression and later pulmonary impairment. Only a few scientific papers have dealt with the effect of impaired pulmonary function on the physical capacity of these adolescents and adults. Most of these studies show small case numbers, inconclusive stress tests, and divergent results.

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.

Conditions

  • Esophageal Atresia

Interventions

DIAGNOSTIC_TEST

Initial Spirometry

Determination of Vital Capacity by spirometry before (within 30 minutes) spiroergometry. Measurements will be performed in both groups.

DIAGNOSTIC_TEST

Final Spirometry

Determination of Vital Capacity by spirometry after (within 30 minutes) spiroergometry. Measurements will be performed in both groups.

DIAGNOSTIC_TEST

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).

DIAGNOSTIC_TEST

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.

DIAGNOSTIC_TEST

Maximum performance

Determination of the maximum performance (W/kg) corrected for body weight by bicycle spiroergometry. Measurements will be performed in both groups.

DIAGNOSTIC_TEST

weight

Determined by Kilogram on a medical weight scale

OTHER

age

Determination of age by patient's Report and past medical history

Sponsors & Collaborators

  • Medical University of Graz

    lead OTHER

Principal Investigators

  • Jana Windhaber, MD · Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria

  • Holger Till, MD · Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria

  • Christoph Arneitz, MD · Department of Paediatric and Adolescent Surgery, Medical University of Graz, Austria

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-08-10
Primary Completion
2019-04-06
Completion
2019-09-02

Countries

  • Austria

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03767673 on ClinicalTrials.gov