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Pharmacokinetics of Glucocorticoids in Children (GLUCOPED)

Completed
Conditions
Children Receiving Prednisone or Prednisolone or Methylprednisolone or Hydrocortisone
Interventions
Biological: Pharmacokinetic
Registration Number
NCT02252237
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

The purpose of this study is to determine individual susceptibility factors (drug interactions, genetic factors such as enzyme polymorphism...) to explain wide interindividual variability towards corticosteroids (prednisone, prednisolone, methylprednisolone, hydrocortisone) in children, which could establish a base for therapeutic monitoring.

Detailed Description

Corticosteroids are widely used in children. A large interindividual variability exists concerning both efficacity and tolerance. Pharmacokinetic is poorly known.

A knowledge of individual susceptibility factors would allow to better adapt therapy in each case.

Drugs evaluated here are used in routine care in children and will be prescribed according to department practices concerning treated disease. Medical checks will be done during usual follow-up. Several features will be collected: reason of treatment, drug chosen and prescription modalities, observance, concomitant treatments, side effects, clinical examination, photography, score... Blood samples will be performed at different interval during usual biological follow-up. Three samples per patient will be required for pharmacokinetic and pharmacogenetic.

170 children under prednisone/prednisolone,130 under methylprednisolone, and 100 children under hydrocortisone will be recruited in four pediatric medical departments: immuno-hematology, nephrology,dermatology, and pediatric neurology.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
146
Inclusion Criteria
  • receiving Prednisone or Prednisolone or Methylprednisolone or hydrocortisone
  • recruited in Immuno-hematological unit, dermatological unit, in pediatric nephrological unit, pediatric intensive care unit, or pediatric neurology unit
  • parental agreement
Exclusion Criteria
  • parental refusal
  • inability to take a blood sample
  • inhaled corticoids intake in the 3 previous days
  • topical corticoids intake in the 3 previous days

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Children with glucocorticoidsPharmacokineticChildren receiving Prednisone or Prednisolone or Methylprednisolone Pharmacokinetic
Primary Outcome Measures
NameTimeMethod
Composite of Pharmacokinetic parameter for Prednisone, Prednisolone, Methylprednisolone, hydrocortisone24 months

Assessed by:

* Volume of distribution of creatinine

* Creatinine clearance

Secondary Outcome Measures
NameTimeMethod
Analysis of genetic polymorphism of proteins taking part in glucocorticoids metabolism24 months
Side effects24 months

Dermaphot® score

Trial Locations

Locations (1)

AP-HP Necker

🇫🇷

Paris, France

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