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Thalassaemia Severity

Thalassaemia Severity Score in Upper Egypt Patients Attending Assuit University Children Hospital

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06720480
Enrollment
85
Registered
2024-12-06
Start date
2024-12-31
Completion date
2025-12-31
Last updated
2024-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thalassaemia

Keywords

Thalassaemia severity score

Brief summary

This study aims to develop a nuanced understanding of thalassemia severity in Upper Egypt by integrating various clinical parameters beyond transfusion frequency. By doing so, it seeks to enhance patient management and ultimately improve quality of life for those affected by this condition.

Detailed description

Thalassemia syndrome classified as hemoglobinopathies, represent one of the most prevalent classes of single-gene disorders globally. The mutations in the HBB gene lead to variable impacts on the production of globin proteins, which in turn affects the overall function of hemoglobin. The genetic variants contribute significantly to the diverse clinical presentations and severity of thalassemia. Traditionally, thalassemia has been categorized into Major, intermediate, and Minor based on the frequency of blood transfusions required for survival It has been observed that anemia may not be the sole determinant of thalassemic disease severity, other factors are also responsible for overall clinical status. Accordingly, clinical conditions of the thalassemia patient, cannot classified based on the transfusion status. Phadke et al. (2006), proposed a classification that considers multiple parameters beyond transfusion status . Similarly, Sripichai et al , (2008) classified HbE/β-thalassemia into the 3 categories of mild, moderate, and severe. Another classification was also introduced by Thalassemia International Federation (TIF) , which 'was bit modification Sripichai et al 2008 . Despite these advancements, existing classifications still tend to simplify thalassemia into three categories Globally, An estimated 1-5% of the global population are carriers of a genetic thalassemia mutation.Although the epidemiology of the various clinical forms remains poorly recognized, the disease is known to be highly prevalent in the area extending from sub-Saharan Africa, through the Mediterranean region and Middle East, to the Indian subcontinent and East and Southeast Asia.Thus, >90% of patients with these disorders live in low- and middle-income countries

Interventions

DIAGNOSTIC_TESTHomglobin Electrophoresis

To diagnose thalassaemia &best method to control disease progress

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
6 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

\- Children and adolescents aged from 18 month to 18 year old. Those with thalassemia

Exclusion criteria

* Non Thalassaemia children

Design outcomes

Primary

MeasureTime frame
Scoring thalassaemia severity1year

Contacts

Primary ContactAlZhraa Gaber Mohamed, Master degree
alzhraagaber@gmail.com800-555-5555
Backup ContactKhalid Ibrahim Abdrahman El-sayeh, Proffesour
K.elsayd@aun.edu.eg0100 548 4357

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026