Current partner codePEPTIDESDE
NCT02364297·Not applicable·INTERVENTIONAL

TIPS in Fundal Variceal Bleeding (the TFB Study)

Status

Unknown

Phase

Not applicable

Enrollment

60

Locations

5

Results

Not posted

Publications

3

Study summary

What the protocol is testing.

In the last years, important advances have been done in the treatment and prevention of fundal variceal bleeding in patients with cirrhosis. Experts agree that the combination of pharmacological and endoscopic therapy (with tissue adhesives) should be the first line therapy in the acute bleeding episode from isolated gastric varices (IGV1) or type 2 gastroesophageal varices (GOV2) varices; whereas transjugular intrahepatic portosystemic shunt (TIPS) is considered a rescue therapy. TIPS has been shown to effectively prevent variceal rebleeding but with a potential increase in the incidence of hepatic encephalopathy and/or liver failure. In this sense, a recent randomized controlled trial (RCT) in esophageal variceal bleeding showed that an early TIPS, performed during the first 72h after patient admission resulted in a significant decrease in failure to control bleeding and early and late rebleeding. Moreover, survival was also significantly increased as well as other portal-hypertension related complications (ascites, spontaneous bacterial peritonitis, hepatorenal syndrome, etc). The present study is directed at comparing the outcome of patients with acute bleeding from fundal varices (IGV1 or GOV2) treated by standard therapy (vasoactive drugs + endoscopic injection of tissue adhesives) with or without early TIPS (performed during the first 1-5 days after admission). Main end-point will be survival free of variceal rebleeding at 1 year from inclusion.

Interventions

Treatment arms and agents.

DEVICE

Early TIPS

TIPS (first 5 days)

Timeline

From registration to results.

  1. First posted

    Feb 18, 2015

  2. Study start

    Sep 2015

  3. Primary completion

    Nov 2018

  4. Study completion

    Dec 2018

  5. Results posted

    Not reported

  6. Registry updated

    Mar 15, 2018

Outcomes

What the study measures.

Primary outcomes

Combined: Absence of rebleeding + survival

Time frame · 1 year

The primary endpoint combines absence of rebleeding + survival during the first 1 year after inclusion in the study. Patients to compare are those with liver cirrhosis and acute bleeding from IGV1 or GOV2 varices initially treated with combined pharmacological and endoscopic therapy. Those patients will be randomized to receive a TIPS or standard medical therapy (pharmacological + endoscopic injection of tissue adhesives)

Secondary outcomes

Absence of portal hypertension-related complications (ascites, spontaneous bacterial peritonitis, hepatorenal syndrome)

Time frame · 6 weeks and 1 year

Comparison of the development of portal-hypertension related complications.

Transfusional requirements

Time frame · 6 weeks and 1 year

We will compare the number of packed red blood cells required by each treatment arms as a surrogate of rebleeding.

Individual adverse events

Time frame · 1 year

Related and not related to the therapies under study.

Hospital stay

Time frame · 1 year

Including the stay for the index bleed and also readmissions due to complications of liver disease.

Use of hospital resources

Time frame · 1 year

Use of hospital resources other than specified in the treatment arms (TIPS, revision of TIPS patency, derivative surgery or additional endoscopic therapy).

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
75 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: Patients developing acute variceal bleeding from GOV2 and/or IGV1 defined according to Baveno II criteria, admitted in the Hospital and receiving standard combined medical therapy (somatostatin 3 mg/12h continuous IV infusion or terlipressin, 2mg/4h IV + endoscopic injection of tissue adhesives as per center protocol). Exclusion Criteria: * Hepatocarcinoma without therapeutic options (according to Milan criteria). * Portal or mesenteric vein thrombosis avoiding the performance of TIPS. * Acute alcoholic hepatitis. * Platelet count \< 20.000/mm3. * Previous treatment with portosystemic shunt. * Pregnancy. * Previous inclusion in the current study. * Terminal liver disease (bilirrubin \> 10 mg/dL and/or prothrombin index \< 30%); or other fatal non-liver diseases. * Denied informed consent.

Study locations

5 registered sites.

Spain. Showing up to 24 locations stored in the fast local snapshot.

Hospital Germans Trias i Pujol

Badalona, Catalonia, Spain

ICU Liver Unit. Hospital Clinic of Barcelona

Barcelona, Catalonia, Spain

Hospital de la Santa Creu i Sant Pau

Barcelona, Catalonia, Spain

Hospital del Mar

Barcelona, Catalonia, Spain

Hospital Arnau de Vilanova

Lleida, Spain

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Related PeptideStat pages

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