Recruiting NCT06591936
Genetic Profile of Alpha Thalassemia Children at Sohag University Hospital .
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Alpha-Thalassemia. Basic parameters: 0 Days — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Genetic profile of alpha thalassemia children at sohag university hospital ,the aim to determine the prevelance , molecular character of the disorder, characterized by decreased synthesis of alpha -globin Recent work to provide mechanisms for phenotypic heterogeneity .
Primary outcome measures
- PCR for prevelance of mutation phenotype [Time frame: one year]
Eligibility criteria
Inclusion criteria
- Acase suspecteed of alpha thalassemia
- age between 0-18years
- micocytic hypochromic anemia not iron deficiency anemia or Beta thalassemia
Exclusion criteria
- Age more than 18 years
- healthy children free from any chronic hematological disease
- micocytic hypochromic anemia either iron deficiency anemia or Beta thalassemia
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Egypt · 1 center
- Sohag University Hospital — Sohag
Identifiers
NCT: NCT06591936 · soh-med-24-08-02MS