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Taking people in EgyptNo phase

Registry of Children and Young People With Sickle Cell Disease in Cairo

Collects records and follows people with sickle cell disease over time, without any treatment.

Plain-language title generated from the registry record
Registry title: Hemoglobin Disorders in Egypt: Sickle Cell Disease Ain Shams University Institutional Registry

Key facts

Where
Cairo, EgyptSee the 2 sites

Where in Egypt

  • Faculty of Medicine Ain Shams Research Institute- Clinical Research CenterCairo, EgyptTaking people
  • Faculty of Medicine-Ain Shams UniversityCairo, EgyptNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Ain Shams University
Trial code
NCT07800247
Record updated
2 September 2026
Original description
This is a retrospective descriptive study to create an institutional registry that will continue as a prospective follow-up non-intervention study that will be carried out at Hematology Oncology and BMT Department, Children's Hospital, Ain-Shams University, Cairo, Egypt.Read full original descriptionShow less

Hemoglobin Disorders in Egypt: Sickle Cell Disease Ain Shams University Institutional Registry

This is a retrospective descriptive study to create an institutional registry that will continue as a prospective follow-up non-intervention study that will be carried out at Hematology Oncology and BMT Department, Children's Hospital, Ain-Shams University, Cairo, Egypt.

Inclusion: children, adolescents and young adults with sickle cell disease.

Exclusion: other inherited anemia.

ClinicalTrials.gov NCT07800247