Direct Oral Novel Anticoagulants for Patients With High-risk Gastroesophageal Variceal Bleeding and Portal Vein Thrombosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorShanghai Zhongshan Hospital

About this trial

This study aims to explore the safety and efficacy of oral administration of a novel anticoagulant (rivaroxaban) in patients with cirrhosis accompanied by high-risk esophagogastric variceal bleeding and portal vein thrombosis, through a prospective, multicenter, randomized controlled clinical trial, starting 48 hours after endoscopic treatment to prevent rebleeding.

Eligibility criteria

Qualifiers

Clinical and imaging diagnosis of liver cirrhosis and esophagogastric varices, with at least one previous episode of esophagogastric variceal bleeding

Combined with portal vein thrombosis and D-dimer > 0.8mg/L

Endoscopic evaluation reveals a high risk of variceal bleeding, and endoscopic treatment is performed to prevent rebleeding of esophagogastric varices

Signed informed consent form

Disqualifiers

Received other antithrombotic therapies before (including warfarin, aspirin, low-molecular-weight heparin, etc.)

Combined with hepatocellular carcinoma or other malignancy

Combined with portal cavernoma

Combined with severe life-threatening diseases of circulatory, hematological and respiratory system

Trial design

Treatments tested in this trial

  • Rivaroxaban

Treatment groups

175 Participants
are divided into 2 treatment groups

Sponsors and collaborators