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NCT Number: NCT07093606

Eltrombopag Induced Liver Dysfunction During Treatment of Immunethrombocytopenic Purpura

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

Recruiting

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Adult patients (≥18 years) diagnosed with primary ITP. Receiving eltrombopag as part of their treatment. Baseline liver function tests (LFTs) within normal limits. Patients with diabetes Patients without diabetes Patients with fatty liver Patients without fatty liver

Exclusion criteria

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

Treatment and study plan

eltrombopag

Drug

ITP patients will receive Eltrombopag and evulate occurance of liver disordres .

Primary outcomes

  1. •To assess the incidence and severity of liver dysfunction in ITP patients receiving eltrombopag.

    Time frame: 3-6 months after receiving eltombopag

    the incidence and severity of liver dysfunction in ITP patients

Study contacts

Contact information is provided by the study sponsor or research team.

Peter A Alfy, Resident

CONTACT

[email protected]

01274069691

Usama M Abdelaal, Professor

CONTACT

01065962094

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 30, 2025
Registry last updated
Jul 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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