The goal of this project is to collect data and blood samples from women with uterine fibroids. For the duration of this project, Dr. Marsh will oversee all activities related to patient enrollment, accrual and all site activities. As the PI of the Clinical Center, Dr. Marsh will be involved in each aspect of the research cycle including ensuring ongoing adherence to the study protocol, supporting selected projects, evaluating data, reviewing enrollment strategies, and providing timely reporting of enrollment data. The Clinical Center study team will work under Dr. Marsh and will be responsible for maintaining and delivering data as outlined in the research proposal. The Clinical Center will establish a close working relationship with DCRI to ensure that the routine collection and delivery of research data is treated as outlined in the protocol. The CC team will work closely with the study PI and the Project Leader to ensure enrollment targets are being met.
|Effective start/end date||9/30/14 → 9/29/19|
- Duke University (1P50HS023418-01)
- Agency for Healthcare Research and Quality (1P50HS023418-01)