Actively Recruiting

Age: 18Years +
All Genders
ID04614961

Database Concerning Patients Consulting the Obesity Clinic of University Hospitals Leuven

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-03

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Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are creating a registry of individuals visiting the Obesity Clinic at the University Hospitals of Leuven to improve understanding of obesity, its treatments, and outcomes. This observational study collects data from patients with overweight, obesity, or those who have undergone bariatric surgery. The registry gathers information from screening and follow-up visits, including sociodemographic details, types of treatments like individual and group lifestyle therapy, medical therapy, and bariatric surgery, along with treatment results. Various assessments such as biochemistry tests, questionnaires, and quality of life measures are included. Participants will have their routine clinical data recorded during their visits, which includes treatment effects and disease impact. The study tracks outcomes over a broad age range, up to 100 years. This ongoing observation aims to collect comprehensive data to better understand obesity and related treatments in real-world settings.

CONDITIONS

Brief Title

Database Concerning Patients Consulting the Obesity Clinic

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent
  • Age 18 years or older
  • Subjects with overweight, obesity or after bariatric surgery
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 100 years

Participants who undergo routine care are observed. Measurements are collected before and after routine healthcare including lifestyle therapy, medical therapy, or bariatric surgery as applicable.

Regular follow-up visits as part of routine care

Trial Site Locations

Total: 1 location

1

Obesity Clinic University Hospitals Leuven

Leuven, Belgium, 3000

Actively Recruiting

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Research Team

B

Bart Van der Schueren, MD, Phd

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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