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Determining of Normal Values and Conformity Assessment of the Dosage of a Plasmatic Marker of the Cellular Captation of Glucose: the IRAP Protein — IRAP  

Insulin Resistance Clinical Trial

Official title:
Determining of Normal Values and Conformity Assessment of the Dosage of a Plasmatic Specific Marker of the Cellular Captation of Glucose: the IRAP Protein (Insulin Regulated AminoPeptidase)

Clinical Trial Summary

The purpose of this study is on one hand to verify the measurement conformity of the IRAP dosage and on the other hand to obtain normal values of the blood IRAP concentration on healthy volunteers.

Clinical Trial Description

This study consists of two visits, from two to five days apart. The first visit : - Healthy volunteers will be on an empty stomach. - they will have a clinical examination, blood tests and blood samples will be taken to constitute a blood collection. the IRAP concentration will be measured with those samples. The second visit : This visit will take place in an interval from 2 to 5 days after the first visit. - Subjects will be on an empty stomach - An oral glucose tolerance test (OGTT) of 3 hours will be performed. Blood samples will be taken three time 15 minutes apart at Baseline (before taking the glucose). And then after the glucose intake, blood sample will be taken every 15 minutes to measure insulinemia, blood glucose, and IRAP concentration. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02941874
Study type Observational
Source University Hospital, Grenoble
Contact
Status Completed
Phase
Start date April 7, 2017
Completion date December 12, 2019
View Details
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