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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02590120
Other study ID # 12.02.FR.NHS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date December 2021

Study information

Verified date March 2022
Source Nestlé
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate amino acid absorption with two different type of proteins.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with gastrointestinal disorder : citrulline plasma concentration < 20 µmol/L and/or xylose plasma concentration < 1,7 mmol/L - Patient under enteral nutrition at home - Patient already receiving 1 L by day Exclusion Criteria: - Obese patient BMI > 30 - Diabetes - Renal or liver failure - Glucocorticoids treatment

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Enteral nutrition


Locations

Country Name City State
France CHU de Lille Lille

Sponsors (1)

Lead Sponsor Collaborator
Nestlé

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amino acid absorption profile Area under the curve of amino acid plasma concentration 48 hours
Secondary Tolerance Description and occurence of adverse events 48 hours
Secondary Nutritional status Retinol Binding Protein and Transthyretin dosage 48 hours
Secondary Essentials amino acid absorption Area under the curve of plasma concentration 48 hours
Secondary Insulinemia evolution Insulinemia dosage 48 hours
Secondary Link between amino acid and insuline Correlation coefficient 48 hours
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