Glycemic Profile by CGMS in Diabetic Patients After Bariatric Surgery
NCT ID: NCT04332354
Last Updated: 2020-04-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
31 participants
OBSERVATIONAL
2016-03-30
2018-05-30
Brief Summary
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Detailed Description
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Judgement criteria are defined as follows: the success of bariatric surgery will be defined as a % EWL \>50%; normalization of glycemia will be defined as a mean 24-hr interstitial glucose level \<100mg/d during the CGM recording period; diabetes remission after metabolic surgery will be defined as an HbA1c level at 1 year after surgery of \< 6.0% without the use of any glucose-lowering agent. Such thresholds were chosen to meet the definition of complete remission by the American Society for Metabolic and Bariatric Surgery and the American Diabetes Association.
Quantitative variables will be expressed as mean + standard deviation. Qualitative variables will be expressed as percentages. Differences in quantitative variables, when compared to the pre-operative period, will be examined using Students t-test for paired data or with ANOVA. Analysis of subgroups will be carried out using Chi-2 test. Identification of predictive factors for diabetes remission will be based on analysis of ROC curves and the calculation of area under the curve data, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), positive and negative likelihood ratio (LR+ and LR-) at different thresholds for each study variable including the pre-operative and post-operative CGM variables and the Add-Diarem score.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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T2D diabetes obese subjects
Patients have T2D diabetes and are candidates for bariatric surgery. They will receive routine cares and follow-up and will have CGM measurement before and 2 weeks following the surgery
routine care. No intervention
no intervention
Interventions
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routine care. No intervention
no intervention
Eligibility Criteria
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Inclusion Criteria
* treated with oral anti-diabetic medication and/or insulin therapy
* candidate for bariatric surgery
Exclusion Criteria
* refusal of bariatric surgery
18 Years
ALL
No
Sponsors
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University Hospital, Caen
OTHER
Responsible Party
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Other Identifiers
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CHU 20-501
Identifier Type: -
Identifier Source: org_study_id
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