Clinical Trials in Egypt / NCT07132515
Recruiting
Phase 4
Efficacy & Safety of Anticoagulants in Cirrhosis ± HCC
NCT07132515 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
CirrhosisHCC - Hepatocellular CarcinomaPortal Vein Thrombosis
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Mansoura University Hospitals | Al Mansurah | Dakahlia Governorate | Recruiting |
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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