Efficacy and Safety of Growth Hormone Treatment in Juvenile Idiopathic Arthritis

NCT ID: NCT00420251

Last Updated: 2007-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

1996-03-31

Study Completion Date

2006-07-31

Brief Summary

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Growth retardation is well known in patients with severe forms of juvenile idiopathic arthritis. Especially those who were under additional treatment with glucocorticoids for high disease activity. The hypothesis is, that treatment with growth hormone can, at leat in part, overcome growth hormone resistance state and increase final height. In a controlled study we follow patients with juvenile idiopathic arthritis with and without growth hormone treatment until final height. Additionally, we are interested in bone density development in those treated with growth hormone.

Detailed Description

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Growth retardation is well known in patients with severe forms of juvenile idiopathic arthritis. Especially those who were under additional treatment with glucocorticoids for high disease activity. This is the case in patients with a polyarticular and a systemic form of juvenile idiopathic arthritis. The permanent consequence is short stature at final height. Up to 30% of these patients will have a final height below the 3rd percentile, even after discontinuation of glucocorticoid treatment. The hypothesis is, that treatment with growth hormone can, at leat in part, overcome growth hormone resistance state and increase final height. In a controlled study we follow patients with juvenile idiopathic arthritis with and without growth hormone treatment until final height. From safety aspects we were interested in the effect of growth hormone on the disease activity. Additionally, we are interested in bone density development in those treated with growth hormone up to final height.

Conditions

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Juvenile Idiopathic Arthritis Still Disease, Juvenile-Onset

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Genotropin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Polyarticular or systemic juvenile idiopathic arthritis,
* Growth velocity below the 25th percentile and or short stature ,
* Treatment with glucocorticoids for at least the previous 6 months before inclusion,
* Prepubertal stage,
* Bone age below 10 in girls and 12 in boys,
* Growth hormone levels after stimulation with clonidine or arginine above 10 ng/ml

Exclusion Criteria

* Previous treatment with growth hormone,
* Endocrinopathy,
* Additional chronic disease beside juvenile idiopathic arthritis,
* Malignant disase,
* Chromosomal aberration or othe syndromal disease,
* Previous treatment with Oxandrolone,
* Small for gestational age,
* Elevated fasting glucose level
Minimum Eligible Age

4 Years

Maximum Eligible Age

14 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

Ludwig-Maximilians - University of Munich

OTHER

Sponsor Role lead

Principal Investigators

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Susanne M Bechtold, MD

Role: PRINCIPAL_INVESTIGATOR

University Children“s Hospital, Munich

Locations

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Center For Rheumatic Diseases in Childhood

Garmisch-Partenkirchen, , Germany

Site Status

Countries

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Germany

References

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Bechtold S, Ripperger P, Muhlbayer D, Truckenbrodt H, Hafner R, Butenandt O, Schwarz HP. GH therapy in juvenile chronic arthritis: results of a two-year controlled study on growth and bone. J Clin Endocrinol Metab. 2001 Dec;86(12):5737-44. doi: 10.1210/jcem.86.12.8083.

Reference Type RESULT
PMID: 11739431 (View on PubMed)

Bechtold S, Ripperger P, Hafner R, Said E, Schwarz HP. Growth hormone improves height in patients with juvenile idiopathic arthritis: 4-year data of a controlled study. J Pediatr. 2003 Oct;143(4):512-9. doi: 10.1067/S0022-3476(03)00390-1.

Reference Type RESULT
PMID: 14571231 (View on PubMed)

Other Identifiers

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13042004

Identifier Type: -

Identifier Source: org_study_id

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