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Sponsored by: |
Emory University |
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Information provided by: | Emory University |
ClinicalTrials.gov Identifier: | NCT00231361 |
This is an observational research study (called a registry) for growth failure. The purpose is to collect information on those who use Genentech growth hormone.
Condition | Intervention |
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Growth Disorders |
Drug: Growth hormone |
Study Type: | Observational |
Study Design: | Natural History, Cross-Sectional, Defined Population, Retrospective Study |
Official Title: | Genentech National Cooperative Growth Study (NCGS) Post Marketing Surveillance Program for Nutropin AQ (Somatropin [rDNA Origin] Injection), Nutropin (Somatropin [rDNA Origin] for Injection) and Protropin (Somatrem for Injection) |
Ages Eligible for Study: | 18 Years to 22 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contact: Melissa Hamilton, BS | 404-785-1717 | Melissa.Hamilton@choa.org |
United States, Georgia | |
Children's Healthcare of Atlanta | Recruiting |
Atlanta, Georgia, United States, 30322 | |
Contact: JoAnn Sadowski, BS 404-785-3531 Joann.Sadowski@choa.org | |
Principal Investigator: Lillian R. Meacham, MD |
Principal Investigator: | Lillian R. Meacham, MD | Children's Healthcare of Atlanta |
Study ID Numbers: | 334-2005 |
Study First Received: | October 3, 2005 |
Last Updated: | December 13, 2006 |
ClinicalTrials.gov Identifier: | NCT00231361 |
Health Authority: | United States: Institutional Review Board |
Growth failure Pediatric population |
Growth Disorders |
Pathologic Processes |