Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:41 AM
Ignite Modification Date:
2025-12-25 @ 1:41 AM
NCT ID:
NCT03975894
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women with sickle cell disease (all genotypes)
* Gestation 18+0 weeks or below
* Willing and able to give informed consent
* Singleton pregnancy
Exclusion Criteria:
* On long term transfusion programme prior to pregnancy for amelioration of SCD
* Prior Hyperhaemolysis
* Red cell phenotype or antibodies present prevent likely provision of adequate red cell units to support elective EBT programme
* Unable to receive blood transfusion for social, religious or clinical reasons
* Current diagnosis of major medical or psychiatric comorbidity which in the randomising clinicians opinion renders them unable to enter trial
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03975894
Study Brief:
Protocol Section:
NCT03975894