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Esophageal Atresia: Metaplasia, Barrett (Oesophagix)

U

University Hospital, Lille

Status

Completed

Conditions

Esophagus, Barrett
Gastroesophageal Reflux

Treatments

Procedure: esophageal biopsies

Study type

Observational

Funder types

Other

Identifiers

NCT02495051
2009/cic
DR-2011-057 / A 910270 (Other Identifier)

Details and patient eligibility

About

The frequency of Barrett's esophagus (BE) has increased in adults in the last decades, but BE is rare in children. Esophageal atresia (EA), the most common congenital anomaly affecting the esophagus, predisposes the patient to severe and prolonged gastroesophageal reflux disease. Because gastroesophageal reflux disease plays a major role in the development of BE by causing repeated mucosal damage, development of BE is a concern even in children and young adults in this specific population. The aim of this study is to assess the prevalence of BE (gastric and/or intestinal metaplasia) in a population of adolescents/young adults who had been treated for EA in early infancy. All eligible patients received upper gastrointestinal endoscopy under general anesthesia with standardized esophageal staged biopsies. Histological suspicion of metaplasia was confirmed centrally.

Enrollment

120 patients

Sex

All

Ages

15 to 19 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medical history of esophageal atresia (all types, Ladd's classification)

Exclusion criteria

  • No medical history of esophageal atresia
  • Non acceptance to participate from the patient and/or his parents
  • esophageal atresia treated with esophageal replacement (e.g., coloplasty, gastric transposition)

Trial design

120 participants in 1 patient group

single group-study
Treatment:
Procedure: esophageal biopsies

Trial contacts and locations

20

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Data sourced from clinicaltrials.gov

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