Plain-English translation of NCT07800247 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This study is creating a database of patients with sickle cell disease at a hospital in Cairo, Egypt. Researchers will start by collecting information from children, teenagers, and young adults who have already been seen at the hospital, and then follow some of these patients over time to track how their condition changes. The goal is to build a better understanding of sickle cell disease in the Egyptian population.
Sickle cell disease affects many people in Egypt, but there is limited organized information about how the disease progresses and affects patients in this population. This registry will help doctors and researchers better understand the disease locally and potentially improve care for future patients.
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If you participate, researchers will review your medical records from the hospital to gather information about your sickle cell disease history, symptoms, and treatments. Some participants may also be followed over time with periodic check-ins to track how you are doing. This is not a treatment study — no new medications or procedures are being tested; instead, the focus is on collecting and organizing information about your health.
AI-generated summary from trial data · Sep 15, 2026 · Not medical advice
Egypt
Enrollment target
~400 participants
Started
March 2024
Primary completion
January 2027
Last updated on clinicaltrials.gov in September 2026.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Dr. Fatma Ebeid Ebeid
Ain Shams University
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.