Status:
COMPLETED
Growth Hormone Treatment in Infants Aged 1 to 2 Years With Chronic Renal Insufficiency (CRI) and Growth Retardation.
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Chronic Kidney Disease
Chronic Renal Insufficiency
Eligibility:
All Genders
9-15 years
Phase:
PHASE4
Brief Summary
This trial is conducted in Europe. Objective(s): To evaluate the effect of human growth hormone on infants aged 1 to 2 years with chronic renal insufficiency (CRI) and growth retardation despite an ad...
Eligibility Criteria
Inclusion
- Patients will be infants of both sexes aged 12 ± 3 months with chronic renal insufficiency and growth retardation.
- To be included in the trial, patients must meet all of the following inclusion criteria a.)-c.):
- a.) Male or female infants with a chronological age of 12 ± 3 months
- b.) Chronic renal insufficiency with Glomerular Filtration Rate less than 60 ml/min./1.73m2, according to the method used routinely in each participating center
- c.) Growth retardation documented at the start of the trial, according to the following criteria: Length less than -2 SDS by chronological age and sex and linear growth velocity \<P50 according to the Hernández standards and to Lubchenko in the case of infants born prematurely (\<37 weeks)
- Conservative treatment or chronic peritoneal dialysis
- Euthyroid
- The parent or guardian must give informed consent to the child's participation in the study before any trial related activities. Trial related activities are any procedures that would not have been performed during the normal management of the subject
- Optimal nutritional management criteria met
- Appropriate metabolic control for severe hyperparathyroidism, hydroelectrolyte balance, acid-base balance and calcium-phosphorus balance
Exclusion
- Any primary endocrinological disorder and severe renal osteodystrophy.Other causes, apart from CRI, giving rise to growth retardation.Hydrocephalus.
- Known or suspected allergy to the trial product or related products.
- Treatment with corticosteroids within the last six months.
- Renal disease due to the Fanconi syndrome or to oxalosis (except if not under dialysis).
- Known or suspected malignancy.
Key Trial Info
Start Date :
January 29 1998
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 21 2005
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT00184769
Start Date
January 29 1998
End Date
December 21 2005
Last Update
February 27 2017
Active Locations (20)
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1
Novo Nordisk Investigational Site
Coimbra, Portugal, 3000-075
2
Novo Nordisk Investigational Site
Lisbon, Portugal, 1160-045
3
Novo Nordisk Investigational Site
Lisbon, Portugal, 1649-035
4
Novo Nordisk Investigational Site
Porto, Portugal, 4200-319