A research registry is a database (data warehouse) where clinical and other related information from patients is collected and stored for medical research. The purpose of this TOS registry is to collect and store medical data ...

You are invited to donate your blood, urine, research data, and related information to be stored (banked) in a research specimen/data database or bank where it can be used for future research projects. The specimens/data collec ...

The purpose of this study is to identify and evaluate changes in blood and bile that may give specific indications of malignant cell metabolism in cancer. Recently, a lot of research has been done to test for certain markers in ...

The project will involve the creation of the Florida Neonatal Neurologic Network. This network will consist of major academic and private hospitals in North-Central Florida linked together with the purpose of creating a robust ...

The purpose of this study is to create a bank of information and outcomes for patients who are part of a weight management program using data collected from medical records.

The complex high acuity-patient population seen in tertiary NICU's located in major children's hospitals across the nation is a unique predominately referral population, not seen in most NICU's supported by in-ho ...

The purpose of this study is to obtain long-term safety information on the disease and medications that you received or are receiving for your Inflammatory Bowel Disease. Crohn’s Disease is characterized by inflammation (the ch ...

NAPRTCS is a research effort that was organized in 1987 by a group of physicians and surgeons committed to the success of pediatric renal transplant.

We are doing this study to look at whether the study medicine (semaglutide) has a positive effect on heart disease in patients that have type 2 diabetes. This will be done by comparing the study medicine (semaglutide) against p ...