NCT07472608

Brief Summary

Obesity medicine, or bariatric medicine, focuses not only on the biological and behavioral aspects, but also on the environmental and social factors that contribute to the development of obesity. Many diseases are associated with obesity, such as type 2 diabetes, hypertension, cardiovascular diseases, numerous cancers, gynecological disorders, etc. Focusing on obesity medicine is crucial for improving patients' quality of life, reducing healthcare costs, and developing effective prevention strategies. The Quebec Heart and Lung Institute - Laval University (IUCPQ-ULaval) maintains a clinical database and biological material bank for studying the multidisciplinary management of obesity and its complications. A biobank is a collection of information, clinical or biochemical data (including radiological, cardiac, and genetic data), and blood samples concerning donors. The information that can be collected includes, for example, age, sex, diagnosis, progression or treatment of a medical condition, medications, DNA, etc. DNA is a molecule present in all cells and contains all the information necessary for the development and functioning of our body. This bank aims to better characterize patients' profile receiving follow-up care in obesity medicine, identify predictive factors of success or failure of interventions and adapt management strategies according to specific needs. The collected data and blood samples will be used in several research projects with the following objectives:

  1. 1.To document the socioeconomic, demographic, clinical, radiological, genetic, and biochemical characteristics of patients living with obesity and requiring medical follow-up at the bariatric medicine clinic at the IUCPQ-ULaval
  2. 2.To explore the effects or associations of genetic and biochemical determinants on health in the context of obesity
  3. 3.To gain a better understanding of the pathophysiology and genes involved in obesity and associated metabolic abnormalities
  4. 4.To evaluate the clinical utility of non-invasive biomarkers in the screening of preclinical obesity and its comorbidities and/or
  5. 5.To evaluate the effectiveness of medications, health behavior changes, and bariatric surgery in order to develop optimal interventions aimed at improving the health and medical management of people with obesity.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25,000

participants targeted

Target at P75+ for all trials

Timeline
304mo left

Started Jun 2026

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 27, 2026

Completed
17 days until next milestone

First Posted

Study publicly available on registry

March 16, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
25 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2051

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2051

Last Updated

March 16, 2026

Status Verified

March 1, 2026

Enrollment Period

25 years

First QC Date

February 27, 2026

Last Update Submit

March 11, 2026

Conditions

Keywords

BiobankClinical dataRadiological dataGenetic dataBiochemical dataCardiac dataBlood samplesProspective patient registryBariatric medicineHealthObesity medicine

Outcome Measures

Primary Outcomes (1)

  • Success or failure of obesity medicine interventions

    1. Anthropometric Parameters: weight and height combined to obtain BMI (kg/m\^2). Waist circumference (cm); Body composition assessed by bioelectrical impedance analysis 2. Cardiometabolic Parameters and Comorbidities: Hepatic steatosis and fibrosis assessed by controlled attenuation parameter (CAP) and liver stiffness measurement (transient elastography); Liver biochemical parameters (e.g., ALT, AST, GGT); Lipid profile (total cholesterol, LDL-C, HDL-C, triglycerides); Inflammatory markers (as available in medical records); Glycemic parameters (fasting glucose, HbA1c, insulin, as available); Polysomnography parameters (when available); Echocardiographic parameters (when available) 3. Adoption of Lifestyle Intervention: Documented adherence and engagement in prescribed lifestyle interventions, as reported in medical charts 4. Quality of Life: Clinician-documented quality-of-life assessment, as recorded in medical charts 5. Mental Health Parameters: As recorded in medical charts

    Baseline to 15-year follow-up. Follow-up is based on standard care consultations which vary from a patient to another

Study Arms (1)

Obesity medicine cohort

This cohort includes patients followed in bariatric medicine at IUCPQ-ULaval

Other: Behavioral and Pharmacological Treatments

Interventions

Behavioral and pharmacological treatments are part of the standard of care and will vary among individuals based on their specific needs.

Obesity medicine cohort

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patient starting follow-up at the Bariatric Medicine Clinic of the IUCPQ-ULaval.

To be included in the registry (database + biobank), a person must first be referred to the Bariatric Medicine Clinic at the IUCPQ-ULaval and meet several criteria: 1. Be over 18 years of age 2. Meet at least one of the following five criteria: 1. Body mass index ≥30 kg/m2 with or without comorbidities (preclinical or clinical obesity); 2. Require weight loss related to a transplant, bariatric surgery, or another type of surgery (e.g., hernia repair, orthopedic surgery, neurosurgery, etc.); 3. History of bariatric surgery resulting in weight regain of at least 15% of the total weight lost; 4. History of bariatric surgery resulting in weight loss deemed insufficient by the treating medical team; 5. Having undergone bariatric surgery with complications related to it (i.e., flushing syndrome or hypoglycemia, nephrolithiasis, return of comorbidities in remission, abnormalities in phosphocalcic balance and vitamin deficiencies).

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Centre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec

Québec, Quebec, G1V 4G5, Canada

Location

Biospecimen

Retention: SAMPLES WITH DNA

Blood samples.

MeSH Terms

Conditions

Obesity

Interventions

Drug Therapy

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Therapeutics

Central Study Contacts

Fannie Lajeunesse-Trempe, MD PhD FRCPC

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
25 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinician-Researcher

Study Record Dates

First Submitted

February 27, 2026

First Posted

March 16, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

June 1, 2051

Study Completion (Estimated)

June 1, 2051

Last Updated

March 16, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations