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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01112228
Other study ID # Clinical Obesity Staging Tools
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2009
Est. completion date August 2011

Study information

Verified date October 2020
Source Imperial College London
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Bariatric surgery
Bariatric surgery: Gastric bypass, Sleeve gastrectomy, or Gastric banding

Locations

Country Name City State
United Kingdom Imperial Weight Centre, Imperial College London London

Sponsors (1)

Lead Sponsor Collaborator
Imperial College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

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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