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Plasma Citrulline Level in Relation to Absorptive Surface

G

Ghent University Hospital (UZ)

Status

Completed

Conditions

Intestinal Failure

Treatments

Procedure: Blood sampling

Study type

Interventional

Funder types

Other

Identifiers

NCT00286039
2005/163

Details and patient eligibility

About

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

Enrollment

200 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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