Database Concerning Patients Consulting the Obesity Clinic of University Hospitals Leuven
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 999,999
- Locations
- 1
- Primary Endpoint
- Routine treatment data (sociodemographics, treatment and treatment outcome, disease impact, biochemistry, questionnaires, ...)
Study Overview
Brief Summary
A registry of individuals that visit the Obesity Clinic of the University Hospitals of Leuven will be established. The objective of this registry is to improve the knowledge about obesity, the treatment of obesity and its outcomes.
Detailed Description
A registry/database is constructed with data of the individuals that visit the Obesity Clinic of the University Hospitals of Leuven. Data will be obtained from the screening visits and all follow-up visits in terms of sociodemographics, treatment and treatment outcomes, disease impact, biochemistry, questionnaires, QoL, ...
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Signed informed consent
- •Age 18 years or older
- •Subjects with overweight, obesity or after bariatric surgery
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Routine treatment data (sociodemographics, treatment and treatment outcome, disease impact, biochemistry, questionnaires, ...)
Time Frame: up to 100 years
The objective is to develop an Obesity Clinic registry to collect routine treatment data (sociodemographics, treatment and treatment outcome, disease impact, biochemistry, questionnaires, ...) using the electronic medical record to improve the knowledge on obesity, the treatment of obesity and its outcomes.
Secondary Outcomes
No secondary outcomes reported