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Recruiting Phase 4

Efficacy & Safety of Anticoagulants in Cirrhosis ± HCC

NCT07132515 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 4
Started
2023-08-15
Last updated
2025-08-20

Condition(s) studied

CirrhosisHCC - Hepatocellular CarcinomaPortal Vein Thrombosis

Investigational drug(s) / intervention(s)

Enoxaparin, warfarrin, or apixaban →

Enoxaparin, warfarrin, or apixaban: Enoxaparin, warfarrin, or apixaban

Study summary

We will give an anticoagulant against portal vein thrombosis, and watch for the results.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Portal vein thrombosis, Cirrhosis, With or without HCC, Child A \& B Exclusion Criteria: * Platelets\<10000, Createnine \>1.9, Budd ciarri, Uncontrolled active bleeding

Primary outcome measure(s)

  • Portal vein thrombosis — 6 months
    determine if thrombus resolved or not on anticcoagulant by triphasic CT

Trial sites (1)

FacilityCityRegionStatus
Mansoura University Hospitals Al Mansurah Dakahlia Governorate Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07132515 on ClinicalTrials.gov ↗ ← All trials in Egypt