| Project/Protocol Title: | Practices and Outcomes of Estrogen Replacement in Pubertal-Aged Girls with Turner Syndrome |
| ClinicalTrials.gov Identifier: | |
| Principal Investigator (PI): | Judith L. Ross |
| Associate Investigators: | Leona Cuttler, Linda diMeglio, Charmian Quigley, Robert Rosenfield |
| Contact Info of PI |
| Mailing Address: | 1025 Walnut St., Suite 726 |
| City: | Philadelphia, PA 19107 |
| State: | PA |
| Zip: | 19107 |
| Phone | 215-955-1648 |
| Fax: | 215-955-1744 |
| E-mail: | Judith.Ross@jefferson.edu |
| Purpose of Study: | To evaluate the prevalence of spontaneous puberty and outcomes of pubertal induction regimens in girls with Turner syndrome (TS), as used in standard pediatric endocrine practice in the USA |
| Location of Study: | 10-15 sites in US that follow at least 5 patients with Turner Syndrome |
| Inclusion Criteria: | "Karyotype diagnosis of Turner syndrome (any karyotype diagnosis of TS is acceptable, including those with a Y-chromosomal component)
"Ages 7-20 years |
| Exclusion Criteria | None |
| Condition(s) |
- Growth Disorders
- Growth Hormone Treatment of Turner Syndrome
- Reproductive Disorders and Contraception
- Estrogen treatment of patients with Turner syndrome
- Delayed puberty
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| Intervention(s) |
No interventions are part of this study. This is an observational, cross-sectional study of pediatric endocrine practice with regard to pubertal induction and pubertal development in girls with Turner syndrome.
Data will be collected on all girls of appropriate age at any endocrine clinic visit within the two-year study enrolment period (2009-2010).
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| Study Phase | |
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