Skip to content

Registry on Obesity Surgery in Adolescents

A Prospective Observational Cohort Study Collecting Coordinated Clinical, Epidemiological, and Behavioural Data to Assess Safety and Efficacy of Surgical Treatment in Adolescent Morbid Obese Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03203161
Acronym
ROSA
Enrollment
50
Registered
2017-06-29
Start date
2019-09-30
Completion date
2029-09-30
Last updated
2019-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent Obesity, Bariatric Surgery, Morbid Obesity

Brief summary

While bariatric surgery is established as a safe and effective alternative with well-defined risks for severely obese adults, little has been published on its use in children. There are many unresolved questions concerning the long-term metabolic and psychological consequences of bariatric surgery in adolescents, and the difference with the adult population. The appropriate timing for bariatric surgery in young people, and the predictors of success and safety still need to be determined. The aim of this long-term prospective study is therefore to establish the safety and efficacy profile of surgical procedures and to clarify whether reductions in morbidity and mortality outweigh the risks of serious surgical complications and lifelong nutritional deficiencies.

Detailed description

The investigators will conduct a prospective observational cohort design study to collect data during standard clinical care of adolescent bariatric patients (younger than 18 years) who were operated (RYGB or SG) for weight loss. Medical, psychological, behavioral, fitness and social data will be collected by medical personnel guided by checklists and prepared questionnaires. All non-invasive and invasive examinations will be performed following the existing protocol of the multidisciplinary group at the hospital (no alteration of normal standard care). Data regarding family environment (birthdays, weight, length, medication, comorbidities, smoking and education of parents and siblings) will also be obtained from caregivers of the patients.

Interventions

PROCEDUREbariatric surgery

Roux-and-Y Gastric Bypass or Sleeve gastrectomy

Sponsors

Queen Fabiola Children's University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* BMI (or projected BMI) \> 40 kg/m² (projected BMI = weight over the age- and gender-specific BMI z-score defined as severe obesity corresponding at a projected BMI of 40 at the age of 18y) OR * BMI ((or projected BMI) \> 35 kg/m² (projected BMI = weight over the age- and gender-specific BMI z-score defined as severe obesity corresponding at a projected BMI of 35 at the age of 18y) + 1 or more of the following obesity-related comorbid conditions: Obstructive Sleep Apnea Syndrome, Non-alcoholic steatohepatitis, type 2 diabetes, hypertension, benign intracranial hypertension. * Minimum 6 months of organized weight loss attempts before surgery (multidisciplinary follow-up) * Completed most of their linear growth (Tanner stage ≥ IV, bone age ≥ 13 years in girls and ≥ 14 years in boys assessed by the Tanner and Whitehouse method) * Capability and willingness to adhere to postoperative guidelines and prolonged surveillance * Informed Consent Form (ICF) signed by patient and parents (or legal guardian)

Exclusion criteria

* psychological/psychiatric disorders that are decompensated or not efficiently treated * severe and unstable eating disorders (e.g. binge-eating) * signs of addictions or addictive behavior (alcohol or substance abuse) * pregnancy or breastfeeding * life-threatening multisystem organ failure * uncontrolled or metastatic malignancy * uncontrolled HIV infection * hypercarbic respiratory failure * active systemic infection or untreated endocrine dysfunction * diseases threatening in the short term or lack of care (self-care or access to family or social support) * medically correctable causes of obesity

Design outcomes

Primary

MeasureTime frameDescription
Resolution rate of baseline comorbidities associated with morbid obesity1 year after bariatric surgerycomorbidities resolution rate will be expressed in %

Secondary

MeasureTime frameDescription
Incidence of treatment-emergent adverse event30 days after bariatric surgeryNumber of Participants With Treatment-Related Adverse Events as Assessed by CTCAE v4.0
Overall mortality rate30 days after bariatric surgeryOverall mortality rate will be expressed in %
Change from baseline in vitamin deficiencies1 year after bariatric surgeryChange in vitamin deficiencies will be expressed in %
Change from baseline in mineral deficiencies1 year after bariatric surgeryChange in mineral deficiencies will be expressed in %
Resolution rate in baseline comorbidities associated with morbid obesity5 years after bariatric surgerycomorbidities resolution rate will be expressed in %
Reduction in BMI1 year after bariatric surgeryBMI will be reported in kg/m\^2
Change from baseline in body mass composition2 years after bariatric surgeryChange in Fat Mass and Lean Body Mass will be reported in kg
Change from baseline in Eating behaviors after bariatric surgery1 year after bariatric surgeryChange in Eating Behaviors behaviors will be assessed by Dutch Eating Behaviour Questionnaire (DEBQ) and will be reported in units on a scale
Change from baseline in quality of life after bariatric surgery1 year after bariatric surgeryChange in Quality of Life will be assessed by PedsQL questionnaire and will be reported in units on a scale
Weight loss1 year after bariatric surgeryweight loss will be reported in kg

Countries

Belgium

Contacts

Primary ContactHenri Steyaert, MD-PhD
henri.steyaert@huderf.be+3224773197
Backup ContactHelena Reusens, MD
helena.reusens@huderf.be+3224773197

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026