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Sponsored by: |
Genentech |
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Information provided by: | Genentech |
ClinicalTrials.gov Identifier: | NCT00097526 |
This study is a multicenter, open-label, postmarketing surveillance study. The substudy will collect information on BMD in adolescents and young adults with GHD or Turner syndrome who are completing GH treatment for statural indications.
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | Bone Mineral Density in Adolescent Subjects With Growth Hormone Deficiency Who Are Completing Treatment With Nutropin AQ, Nutropin, or Protropin in the National Cooperative Growth Study (NCGS) |
Ages Eligible for Study: | up to 17 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
primary care clinic
Inclusion Criteria:
Exclusion Criteria:
Contact: Trial Information Support Line | 800-723-6247 |
United States, California | |
Trial Information Support Line | Recruiting |
South San Francisco, California, United States, 94080 | |
Contact 800-723-6247 |
Study Director: | Barbara Lippe, M.D. | Genentech |
Responsible Party: | Genentech, Inc. ( Clinical Trials Posting Group ) |
Study ID Numbers: | 85-036, Substudy 10 |
Study First Received: | November 24, 2004 |
Last Updated: | July 14, 2008 |
ClinicalTrials.gov Identifier: | NCT00097526 |
Health Authority: | United States: Institutional Review Board |
Growth Hormone Deficiency |
Chromosomal abnormalities Bone Diseases, Endocrine Dwarfism Hypopituitary dwarfism Genital dwarfism Gonadal Disorders Dwarfism, Pituitary Brain Diseases Bone Diseases Sex Differentiation Disorders Gonadal dysgenesis Urogenital Abnormalities Hypopituitarism Musculoskeletal Diseases Bone Diseases, Developmental |
Congenital Abnormalities Hypothalamic Diseases Pituitary Diseases Chromosome Disorders Endocrine System Diseases Central Nervous System Diseases Monosomy X Growth hormone deficiency Turner Syndrome Genetic Diseases, Inborn Turner syndrome Ovarian dwarfism Endocrinopathy Gonadal Dysgenesis |
Pathologic Processes Disease Syndrome Nervous System Diseases Sex Chromosome Disorders |