Assess the Possibility of Diagnosing Diabetes and Rediabetes Following Oral Induced Hyperglycemia in Patients With Dunnigan's Partial Familial Lipodystrophy by Replacing 75 g of Glucose With a Standardized Carbohydrate Breakfast and Continuous Interstitial Monitoring Glucose)
NCT ID: NCT05789251
Last Updated: 2024-08-21
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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RECRUITING
NA
60 participants
INTERVENTIONAL
2023-06-19
2025-06-30
Brief Summary
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In the literature, different avenues have been explored. First, given oral glucose intolerance, replacement with a standardized breakfast has been explored in several studies. Another alternative tested in the population of subjects with cystic fibrosis is the use of an interstitial glucose sensor for screening for carbohydrate abnormalities.
In view of the literature, we formulate several hypotheses that will be tested in our study:
1. The intake of a standardized breakfast containing 75g of carbohydrates is comparable to the ingestion of 75g of glucose on the result of the OGTT test at 120 min for the diagnosis of carbohydrate abnormalities (diabetes and prediabetes) in patients with Dunnigan's lipodystrophy.
2. The continuous recording of interstitial glycaemia over several days allows the diagnosis of glucidic abnormalities equivalent to the classic OGTT in this population; possibly by identifying glycemic variations not seen by a single OGTT test. Thus the installation of an interstitial sensor over several days could be an alternative to the realization of the OGTT in the identification of carbohydrate disorders in patients with Dunnigan's lipodystrophy.
3. There will be a similar profile but a time lag between venous glycemic curves and interstitial blood glucose measurements after OGTT.
4. Replacing the oral glucose load of the classic OGTT (gold standard) with a standardized carbohydrate breakfast leads to similar interstitial glycaemia curves but with a time lag.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Standardized breakfast to replace in fine oral induced hyperglycemia test
Standardized breakfast to replace in fine oral induced hyperglycemia test
Standardized breakfast
Standardized breakfast to replace in fine oral induced hyperglycemia test
Interventions
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Standardized breakfast
Standardized breakfast to replace in fine oral induced hyperglycemia test
Eligibility Criteria
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Inclusion Criteria
Aged 18 to 75 Having given their informed consent.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de la Réunion
OTHER
Responsible Party
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Locations
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Centre Hospitalier Universitaire de La Réunion
Saint-Denis, , Reunion
Countries
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Facility Contacts
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Other Identifiers
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2023/CHU/03
Identifier Type: -
Identifier Source: org_study_id
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