Biotinidase deficiency |
Carboxylase Deficiency, Multiple, Late-Onset; Multiple Carboxylase Deficiency, Late-Onset |
Clinical Trial: Endocrine Dysfunction and Growth Hormone Deficiency in Children with Optic Nerve Hypoplasia.
This study is currently recruiting patients.
Verified by Children''''s Hospital Los Angeles August 2005
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Purpose
Hypotheses:
- The prevalence of endocrinopathies, and growth hormone (GH) deficiency in particular, among young children diagnosed with optic nerve hypoplasia (ONH) is higher than is commonly thought.
- Early treatment of children with ONH and GH-deficiency can prevent adverse outcomes.
Aims:
- Determine the prevalence and types of endocrinopathies in children diagnosed with ONH.
- Correlate endocrine outcome with radiographic, ocular, and developmental findings in children with ONH.
- Examine the effect of GH treatment on growth and obesity in children with ONH, GH-deficiency, and either subnormal or normal growth compared to children with ONH that are not GH-deficient.
- Compare growth outcomes between children with isolated GH-deficiency and those with multiple hormone deficiencies.
| Condition | Intervention | Phase |
|---|---|---|
| Optic Nerve Hypoplasia Growth Hormone Deficiency Septo-Optic dysplasia Hypopituitarism | Drug: Nutropin AQ | Phase IV |
MedlinePlus related topics: Birth Defects; Dwarfism; Eye Diseases; Head and Brain Malformations; Neurologic Diseases; Pituitary Disorders
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Secondary Outcomes: Endocrine outcomes as correlated with radiographic, ocular, and developmental findings.
Expected Total Enrollment: 38
Study start: December 2004
Subjects for this study will be recruited from active and newly enrolled subjects in our larger ONH study. The study duration is two years and we anticipate 38 subjects will enroll. Subjects will be recruited for this study if they present with either growth deceleration or at least one subnormal result for IGF-1 or IGFBP-3.
Baseline information collected includes: height, weight, head circumference, examinations by an endocrinologist and ophthalmologist, endocrine laboratory testing, fundus photography, electrophysiology testing, head MRI, and a developmental assessment. A glucagon stimulation test will be performed and subjects who are deemed GH-deficient and who have delayed growth will be assigned to GH treatment, in line with standard clinical practice. Those with normal growth but determined to be GH-deficient by a glucagon stimulation test will be randomized to treatment with GH vs observation only.
Subjects randomized to treatment with GH will be provided with GH for the duration of their participation in the study. Enrolled subjects will return every four months to monitor progress. Subjects will undergo a physical examination at each visit, including height, weight, head circumference, and body fat. In addition, subjects randomized to growth hormone will have laboratory testing of thyroid, IGF-1 and IGFBP-3 hormones, and fasting lipid levels.
Eligibility
Inclusion Criteria:
- New subjects diagnosed with ONH less than or equal to 2 years of age and subjects actively enrolled (in currently approved prospective ONH study) will be eligible for enrollment.
Exclusion Criteria:
Location and Contact Information
California
Childrens Hospital Los Angeles, Los Angeles, California, 90027, United States; Recruiting
Mark Borchert, MD, Principal Investigator
Mark Borchert, MD, Principal Investigator, Childrens Hospital Los Angeles; University of Southern California
Mitchell Geffner, MD, Principal Investigator, Children''''s Hospital Los Angeles
More Information
Last Updated: August 31, 2005
Record first received: August 31, 2005
ClinicalTrials.gov Identifier: NCT00140413
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-06

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