Not yet taking people in United StatesNo phase
Building a Database of Health Information From Adults With Sickle Cell Disease
Collects health and treatment information from adults with sickle cell disease.
Plain-language title generated from the registry record
Registry title: Data Collection For Patients With Sickle Cell Disease
Key facts
- Where
- Houston, United StatesSee the site
Where in United States
- UT MD Anderson Cancer CenterHouston, United StatesNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- M.D. Anderson Cancer Center
- Trial code
- NCT07911618
- Record updated
- 3 November 2026
- Original description
To create a database of clinical information, participant /disease characteristics, and treatment history collected from patients with Sickle Cell Disease.Read full original descriptionShow less
Data Collection For Patients With Sickle Cell Disease
To create a database of clinical information, participant /disease characteristics, and treatment history collected from patients with Sickle Cell Disease.
Inclusion: Participants 18 years of age and older diagnosed with Sickle Cell Disease; Participants treated at UT Physicians Sickle Center Cancer Center; Participants treated at UT MD Anderson Cancer Center.