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The Effect of Anticoagulation in Cirrhotic Patients With Portal Vein Thrombosis:A Multicenter RCT

Effect of Anticoagulation After Endoscopic Therapy in Cirrhotic Patients With Portal Vein Thrombosis:A Zelen-design Multicenter Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02630095
Enrollment
96
Registered
2015-12-15
Start date
2015-12-31
Completion date
2018-09-30
Last updated
2015-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Cirrhosis, Portal Vein Thrombosis

Keywords

anticoagulation

Brief summary

The purpose of this study is to determine the effect and safety of anticoagulation after endoscopic therapy in cirrhotic patients with portal vein thrombosis and to explore its effect on long-term rebleeding rate and mortality.

Detailed description

The treatment of cirrhotic patients with PVT (portal vein thrombosis) is clearly recommended in guideline now. Several published studies has confirm the effect and safety of anticoagulation therapy in cirrhotic patients with PVT.The present studies are most observation studies with small sample size and low quality. The investigators need more high-quality research such as randomized controlled trials. This is a Zelen-designed multicenter randomized controlled trial. Patients will randomly enter into two groups:the anticoagulation group or the control group and then the investigator will make sure wether their are fond of the group and make decision by themselves. The recanalization rate and complications will be analyzed

Interventions

Patients will take warfarin started at a dose of 2.5mg/d and with titration of dose to maintain a target INR of 2-3, and during the of perioperative period of Endoscopic treatment changing to use Nadroparin Calcium 4100IU/d,subcutaneous.

DEVICEDoppler ultrasound and CT

all patient will take Doppler ultrasound examination every 3 months ;Abdominal CT will be done every 6 months。

Sponsors

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Shanghai Public Health Clinical Center
CollaboratorOTHER_GOV
ShuGuang Hospital
CollaboratorOTHER
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Shanghai Pudong New Area Gongli Hospital
CollaboratorOTHER
Eastern Hepatobiliary Surgery Hospital
CollaboratorOTHER
Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18-70 years old; * A clinical, radiological or histologic diagnosis of Liver cirrhosis and portal hypertension; * Diagnosed of Portal vein thrombosis; * Capable of understanding the purpose and risks of the study and informed consent to participate in the study; * Have undergone endoscopy to prevent variceal rebleeding.

Exclusion criteria

* Age \<18 or \>70 years; * Portal vein thrombosis diagnosed before 6 months; * Patients with signs of acute PVT such as fever,abdominal pain or intestinal obstruction,who should be treated immediately; * Pregnant or nursing; * Hepatocellular carcinoma or other cancer; * Severe cardiopulmonary diseases or concomitant renal insufficiency; * cavernous transformation of the portal vein; * Contradictions to endoscopy; * Contradictions to anticoagulation,such as:allergy to LMWH or warfarin, severe uncontrolled hypertension, history of hemorrhagic cerebral vascular accident, recent peptic ulcer disease, bacterial endocarditis, ulcerative colitis,sustained platelet count \< 50 x10\^9/L); * Taking immunosuppressive agent; * Coagulation disorders other than the liver disease related; * Variceal bleeding failed to control.

Design outcomes

Primary

MeasureTime frameDescription
Recanalization rate of PVTthrough study completion,an average of 18 monthsPatients will receive Doppler ultrasound and CT before enrolled and followed up by Doppler ultrasound every 3 months ,by CT every 6 months after enrolled,untill the end of the study.

Secondary

MeasureTime frameDescription
Rebleeding ratethrough study completion,an average of 18 monthsThe investigators observe the variceal rebleeding events during the study
Incidence rate of complicationsthrough study completion,an average of 18 monthsThe investigators observe any severe adverse events caused by anticoagulation therapy or the progress of thrombosis.

Countries

China

Contacts

Primary ContactShiyao Chen, Professor
chen.shiyao@zs-hospital.sh.cn86-13601767310

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026