NCT07911618Not yet recruiting
Data Collection For Patients With Sickle Cell Disease
Source: ClinicalTrials.gov · Last updated 3 Nov 2026
Brief summary (registry, in English)
To create a database of clinical information, participant /disease characteristics, and treatment history collected from patients with Sickle Cell Disease.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 500 (estimated)
- First submitted
- 28 Oct 2026
- Start date
- 6 Apr 2027
- Primary completion date
- 1 Jan 2035
- Lead sponsor
- M.D. Anderson Cancer Center
- Diseases
- Sickle cell disease
- NCT number
- NCT07911618
What you commit to
- Study type: Observational
- Planned participants: 500
- From 6 Apr 2027 to the primary completion date, 1 Jan 2035
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| UT MD Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.