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Efficacy & Safety of Anticoagulants in Cirrhosis ± HCC

M

Mansoura University

Status and phase

Enrolling
Phase 4

Conditions

Cirrhosis
HCC - Hepatocellular Carcinoma
Portal Vein Thrombosis

Treatments

Drug: Enoxaparin, warfarrin, or apixaban

Study type

Interventional

Funder types

Other

Identifiers

NCT07132515
MS.23.07.2479

Details and patient eligibility

About

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

Enrollment

100 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 3 patient groups

Anticoagulant in cirrhosis with HCC
Experimental group
Description:
HCC patient on anticogulant like Enoxaparin (clexan), warfarrin(marivan), or DOAC(apixaban)
Treatment:
Drug: Enoxaparin, warfarrin, or apixaban
Anticoagulant in Cirrhosis without HCC
Experimental group
Description:
Benign thrombus in cirrhotic patient on anticoagulant like Enoxaparin (clexan), warfarrin(marivan), or DOAC(apixaban)
Treatment:
Drug: Enoxaparin, warfarrin, or apixaban
No anticoagualnt in Cirrhosis with or without HCC
No Intervention group
Description:
cirrhotic patients with thrombosis with or without HCC not on anticoagulant

Trial contacts and locations

1

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Central trial contact

Hatem Elalfy, PhD; Dalia Elsayed Ganady, MBBS

Data sourced from clinicaltrials.gov

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