Morbid Obesity Clinical Trial
— COSTOfficial title:
Assessing Clinical Staging Tools for Tracking the Impacts of Obesity on Individuals
Verified date | October 2020 |
Source | Imperial College London |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study will assess various published staging tools to assess the health impacts of obesity on individuals. The aim is to identify benefits and drawbacks, and thus help Obesity Centres and GPs better assess obese individuals as well as better identify who benefits most from having weight loss treatment.
Status | Completed |
Enrollment | 600 |
Est. completion date | August 2011 |
Est. primary completion date | August 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years and older |
Eligibility | Inclusion Criteria: - Morbid obesity - At least 1 year follow-up after bariatric surgery Exclusion Criteria: - N/A |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Imperial Weight Centre, Imperial College London | London |
Lead Sponsor | Collaborator |
---|---|
Imperial College London |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in Obesity Scores After Weight Loss Treatment | Changes were measured in the following clinical domains
-Airway, Body Mass Index, Cardiovascular risk, Diabetes, Economic, Functional. Gonadal, Body Image. An improvement was considered when any 1 of these domains changes for the positive. Thus, if a patient had an improvement in cardiovascular risk the intervention was considered beneficial even if no other domains changed. Out measure is calculated as the count of participants achieving at least 1 improvement (Count) |
Minimum of 1 year follow-up | |
Secondary | Changes in Obesity Scores in Various Subgroups | Changes in obesity scores in patients with carious co-morbid conditions (eg, type 2 diabetes, sleep apnoea) before bariatric surgery | Minimum of 1 year follow-up |
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