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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00592735
Other study ID # SVH H06/151
Secondary ID SVH H06/151
Status Completed
Phase N/A
First received January 1, 2008
Last updated June 5, 2016
Start date May 2007
Est. completion date May 2012

Study information

Verified date June 2016
Source Garvan Institute of Medical Research
Contact n/a
Is FDA regulated No
Health authority Australia: Human Research Ethics Committee
Study type Observational

Clinical Trial Summary

This study will follow ,morbidly obese subjects as they undertake weight loss before and after laparoscopic gastric banding, examining markers of glucose and lipid metabolism, adipokines and measures of body fat.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- morbidly obese subjects with type 2 diabetes or metabolic syndrome

- age <70

Exclusion Criteria:

- contra-indications to bariatric surgery

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
laparoscopic gastric banding
standard surgical procedure

Locations

Country Name City State
Australia St Vincent's Hospital Sydney New South Wales

Sponsors (1)

Lead Sponsor Collaborator
Garvan Institute of Medical Research

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary weight loss 6 months No
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