Survey on bariatric surgery for adolescents
Evaluation of the Efficiency and Complications Associated With the Surgical Treatment of Obesity by Laparoscopic Adjustable Gastric Banding in an Adolescent Population.
This study is trying to see how well laparoscopic adjustable gastric banding works for teenagers aged 14-20 who are having bariatric surgery, focusing on weight loss and any health issues that might come up.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 14 Years to 20 Years |
| Sex | All |
| Sponsor | University Hospital, Angers Government |
| Locations | 1 site (Angers, Maine Et Loire) |
| Trial ID | NCT04766801 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather data on the effectiveness and safety of laparoscopic adjustable gastric banding in adolescents aged 14-20 who are candidates for bariatric surgery. It focuses on monitoring weight loss outcomes and the incidence of obesity-related comorbidities, as well as any medical, psychological, and surgical complications that may arise from the procedure. The study builds on previous recommendations from health authorities and seeks to enhance the management of adolescent patients undergoing this treatment. Conducted at the Angers University Hospital, it leverages their expertise in adolescent bariatric surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adolescents aged 14-20 with a BMI of 40 or higher, or 35 or higher with significant obesity-related comorbidities.
Not a fit: Patients with unstable psychiatric disorders or those who do not meet the pre-operative program requirements may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term effectiveness and safety of bariatric surgery in adolescents, potentially improving treatment protocols.
How similar studies have performed: While there have been studies on bariatric surgery in adults, this specific focus on adolescents is relatively novel and under-researched.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Angers, Maine Et Loire
- University Hospital of Angers — Angers, Maine Et Loire, France (Recruiting)
Study contacts
- Principal investigator: Françoise Schmitt, MD-PhD — University Hospital of Angers
- Study coordinator: Françoise Schmitt, MD-PhD
- Email: FrSchmitt@chu-angers.fr
- Phone: 0241354290
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.