Registry of patients visiting the Obesity Clinic
Database Concerning Patients Consulting the Obesity Clinic of University Hospitals Leuven
This study is creating a registry of people visiting the Obesity Clinic to gather information that can help improve treatment and care for obesity.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 999999 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Universitaire Ziekenhuizen KU Leuven Academic / other |
| Locations | 1 site (Leuven) |
| Trial ID | NCT04614961 on ClinicalTrials.gov |
What this trial studies
This observational study establishes a registry of individuals who consult the Obesity Clinic at the University Hospitals of Leuven. It aims to gather comprehensive data from screening and follow-up visits, including sociodemographics, treatment methods, outcomes, disease impact, and quality of life. The collected information will enhance understanding of obesity and its treatment, potentially leading to improved patient care and outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 years or older who are overweight, obese, or have undergone bariatric surgery.
Not a fit: Patients who are under 18 years old or do not have a diagnosis of overweight or obesity will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could provide valuable insights that lead to better treatment strategies for obesity and its related conditions.
How similar studies have performed: Other studies utilizing similar registry approaches have shown success in improving treatment outcomes for obesity, indicating that this method is both tested and effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Signed informed consent * Age 18 years or older * Subjects with overweight, obesity or after bariatric surgery
Where this trial is running
Leuven
- Obesity Clinic University Hospitals Leuven — Leuven, Belgium (Recruiting)
Study contacts
- Study coordinator: Bart Van der Schueren, MD, Phd
- Email: bart.vanderschueren@uzleuven.be
- Phone: +32 16 34 69 94
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.