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NCT00286039 Clinical Trial

Plasma Citrulline Level in Relation to Absorptive Surface

Intestinal Failure Clinical Trial

Official title:
Plasma Citrulline Level in Relation to Absorptive Surface

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00286039
Other study ID # 2005/163
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2005
Est. completion date September 2010

Study information
Verified date July 2021
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Correlation between determination of citrulline in plasma or dried blood Reference ranges for healthy children and babies Longitudinal follow-up of citrulline in preterm babies

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date September 2010
Est. primary completion date September 2010
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - 0-18 years - preterm babies up to 1.500g - preterm babies over 1.500g Exclusion Criteria: - gastro-intestinal problems (except for the preterm babies) - congenital metabolic disorders - dysfunction of the liver or kidneys - congenital defects

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Blood sampling
Blood sampling is used.

Locations
Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Correlation between determination of citrulline in plasma or dried blood Untill end of study
Primary Reference ranges for healthy children and babies Until end of study
Primary Longitudinal follow-up of citrulline in preterm babies Untill end of study
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