Clinical Study Details
Title | Sponsored multicenter depot lupron study |
Description | This multicenter company-sponsored study randomizes children with central precocious puberty (starting in girls before 8 and boys before 9) to two different doses (11.25 mg and 30 mg) of 3 month depot lupron. The study has visits in the General Clinical Research Center every month for the first three months and then every 3 months. All study requirements and medication are provided by the sponsor. Enrollment is expected to close by early autumn 2009. |
Eligibility | To be eligible for this study you must: |
Procedures | |
Contact | Contacts: Dr Kirk Neely and Eileen Durham RN" |