Sickle Cell Research Registry

Sickle Cell Research Registry — Researchers are currently collecting information about the care sickle cell disease patients receive, the medications they are prescribed, as well as the complications they experience. People with sickle cell disease, newborn to age 21, may qualify for enrollment. More about the sickle cell research registry. Contact Diana Ross, MSN, Research Nurse Coordinator — Diana.Ross@chp.edu or 412-692-7857 — to learn about eligibility for this study.