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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03139864
Other study ID # CHU-0292
Secondary ID 2016-A01837-44
Status Recruiting
Phase N/A
First received
Last updated
Start date April 4, 2017
Est. completion date December 2019

Study information

Verified date February 2019
Source University Hospital, Clermont-Ferrand
Contact Patrick LACARIN
Phone 04 73 75 11 95
Email placarin@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The type 1 diabetes is a common chronic disease characterised by the stop of production of insulin by the pancreas. A lot of factors modify blood glucose. The objective is to study the effect of type 1 diabetes on the use of energy substrates (fats and carbohydrates) during exercise of increasing intensity by a comparison with non-diabetic controls children.


Description:

The type 1 diabetes is a common chronic disease characterised by the stop of production of insulin by the pancreas. A lot of factors modify blood glucose. The objective is to study the effect of type 1 diabetes on the use of energy substrates (fats and carbohydrates) during exercise of increasing intensity by a comparison with non-diabetic controls children.


Recruitment information / eligibility

Status Recruiting
Enrollment 48
Est. completion date December 2019
Est. primary completion date May 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 12 Years
Eligibility Inclusion Criteria:

- Children between 6 and 12 years

- Tanner stage <T2

- Type 1 diabetes for more than 1 year for infants with type 1 diabetes

Exclusion Criteria:

- Tanner stage > ou = T2

- Obesity

- Hormonal disease

- Disease who prevent doing exercise

Study Design


Intervention

Procedure:
controlled physical activity
Comparison between infants with type 1 diabetes and infants without type 1 diabetes during exercise :

Locations

Country Name City State
France CHU Clermont-Ferrand Clermont-Ferrand

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of substrate utilization between infants with type 1 diabetes and infants without type 1 diabetes during exercise Measurements will be carried out by indirect calorimetry and the relationship between CO2 et O2 (Metamax) at day 1
Secondary hormonal regulation of blood glucose insulin, glucagon, adrenaline, cortisol and growth hormone will be metered according to their half life until 2 hours after physical activity (T12, T20, T40, T60, T120) at day 1
Secondary lipoxmax : the intensity for wich lipid oxydation is maximum will be carried out by indirect calorimetry during exercise at day 1
Secondary Comparison between infants during 10 days before and 4 days after exercise of blood glucose modification Comparison of curves of interstitial blood glucose measured with Freestyle® 10 days before and 4 days after exercise of blood glucose modification
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