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Thrombophilia In Beta Thalassemia

NCT04219449 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2024-05-07

No results posted yet for this study

Summary

β-thalassemia disease is one of the most common congenital hemolytic anemia commonly found in the malarial belt areas including the Mediterranean, the Middle East, Africa, Southeast Asian countries, and China.

Conditions

Interventions

DIAGNOSTIC_TEST

PT

measuring PT drawn on citrated blood sample

DIAGNOSTIC_TEST

Protein C

measuring protein C drawn on citrated blood sample

DIAGNOSTIC_TEST

Platelet aggregation by ADP and arachidonic acid

measuring platelet aggregation drawn on citrated blood sample

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Eligibility

Min Age
4 Years
Max Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-07
Primary Completion
2024-05-30
Completion
2024-05-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04219449 on ClinicalTrials.gov