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Adolescents Bariatric Surgery Cohort Survey (BariAdo)

U

University Hospital, Angers

Status

Enrolling

Conditions

Obesity, Adolescent
Bariatric Surgery Candidate
Obesity, Morbid

Treatments

Procedure: Laparoscopic adjustable gastric banding

Study type

Observational

Funder types

Other

Identifiers

NCT04766801
2007-06

Details and patient eligibility

About

Obesity affects 3%-4% of the pediatric population and leads to cardiac mortality during adult life. Bariatric surgery is the best treatment for weight loss and preventing obesity associated comorbidities in adults, but its applications and safety are yet to be defined for adolescents.

Full description

Since 2008, in France, certain university hospitals have been eligible to perform bariatric surgery for adolescents. It was therfore possible to define its feasibility, potential complications and specific indications.

This led to recommandations published by Health Authorities (HAS) in 2016. However, it seems imperative to continue monitoring these patients in order to improve their management, especially as the use of these surgical techniques becomes increasingly widespread.

The Angers University Hospital is one of the leading hospitals when it comes bariatric surgery for adolescents through its use of gastric bands.

The aim of this protocol is to update data on how effective this surgery is on weight loss and obesity-associated comorbidities, and to monitor medical, psychological and surgical complications associated with this treatment.

Enrollment

100 estimated patients

Sex

All

Ages

14 to 20 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 14-20 years of age and asking for bariatric surgery
  • BMI >= 40 Kg.m-2 or >= 35 Kg.m-2 with major obesity-related comorbidities (hypertension, diabetes, sleep apnea, etc...)

Exclusion criteria

  • An unstable psychiatric disorder
  • Bariatric surgery anesthesic contraindications
  • Having not completed a minimum of six months of the pre operative program
  • Lack of consent from the patient or the patient's relatives.

Trial contacts and locations

1

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Central trial contact

Françoise Schmitt, MD-PhD; Régis Coutant, MD-PhD

Data sourced from clinicaltrials.gov

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