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Eltrombopag Induced Liver Dysfunction During Treatment of Immunethrombocytopenic Purpura

Not Applicable
Recruiting
Conditions
ITP - Immune Thrombocytopenia
Interventions
Registration Number
NCT07093606
Lead Sponsor
Sohag University
Brief Summary

this study amis to assess the incidence and severity of liver dysfunction in ITP patients receiving eltrombopag.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

Pre-existing liver disease (e.g., hepatitis, cirrhosis, NAFLD). Concurrent use of hepatotoxic drugs. Patients lost to follow-up.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
this group will receive Eltrombopag tabeltsEltrombopagITP patients in this group receive Eltrombopag then follow up by liver functions test to evulate occurance of liver disorders .
Primary Outcome Measures
NameTimeMethod
•To assess the incidence and severity of liver dysfunction in ITP patients receiving eltrombopag.3-6 months after receiving eltombopag

the incidence and severity of liver dysfunction in ITP patients

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sohag university hospital

🇪🇬

Sohag, Egypt

Sohag university hospital
🇪🇬Sohag, Egypt
Magdy M Amin, Professor
Contact

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