- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04614961
Database Concerning Patients Consulting the Obesity Clinic
October 18, 2022 updated by: Universitaire Ziekenhuizen KU Leuven
Database Concerning Patients Consulting the Obesity Clinic of University Hospitals Leuven
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.
Study Overview
Status
Recruiting
Conditions
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 Type
Observational
Enrollment (Anticipated)
999999
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Leuven, Belgium, 3000
- Recruiting
- Obesity Clinic University Hospitals Leuven
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Subjects with overweight, obesity or after bariatric surgery
Description
Inclusion Criteria:
- Signed informed consent
- Age 18 years or older
- Subjects with overweight, obesity or after bariatric surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients with overweight, obesity or after bariatric surgery
|
Medical therapy
Individual therapy
Group therapy
Surgical and endoscopic therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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.
|
up to 100 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 12, 2019
Primary Completion (Anticipated)
December 31, 2099
Study Completion (Anticipated)
December 31, 2099
Study Registration Dates
First Submitted
October 5, 2020
First Submitted That Met QC Criteria
October 28, 2020
First Posted (Actual)
November 4, 2020
Study Record Updates
Last Update Posted (Actual)
October 19, 2022
Last Update Submitted That Met QC Criteria
October 18, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- S62590
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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