Status:
UNKNOWN
Perioperative Evaluation of Glucose Profile Using Continuous Glucose Monitoring System in Glucose Intolerant Patients
Lead Sponsor:
University Hospital, Lille
Conditions:
Hyperglycaemia (Diabetic)
Bariatric Surgery Candidate
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The recent use of a pre-operative carbohydrate loading compared to fasting has been shown to improve the early recovery after surgical procedures by reducing the profound stress response following sur...
Detailed Description
Bariatric surgery allows weight loss and obesity related comorbidities remission. In patients with type 2 diabetes (T2D), glucose intolerance (GI) and metabolic syndrome (MS), weight loss surgery impr...
Eligibility Criteria
Inclusion
- Bariatric surgery planned (RYGB or SG)
- BMI at least 35 kg/m2 with comorbidity that can be improved after surgery(including cardiovascular disease including high blood pressure, obstructive sleep apnea syndrome and other severe respiratory disorders, severe metabolic disorders, particularly type 2 diabetes, disabling osteoarticular disease, steatohepatitis non-alcoholic)
- Glucose Intolerance as defined by the American Diabetes Association (ADA Diabetes Care 2017)
- Negative pregnancy test
- Informed consent
- Patient with social insurance
Exclusion
- Patients receiving insulin therapy
- Previous bariatric surgery
- Definite symptoms of gastroparesis assessed by Gastroparesis Cardinal Symptoms Index (GCSI)\*. Values of score ≥ 1.90 will be chosen as definite symptoms of gastroparesis.
- Pregnant or breastfeeding woman, persons deprived of their liberty, persons under guardianship or trusteeship
Key Trial Info
Start Date :
September 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2024
Estimated Enrollment :
76 Patients enrolled
Trial Details
Trial ID
NCT04343040
Start Date
September 1 2022
End Date
December 1 2024
Last Update
March 15 2022
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