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TIPS in Fundal Variceal Bleeding (the TFB Study) (TFB)

Primary Purpose

Portal Hypertension, Bleeding Gastric Varices

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Early TIPS
Sponsored by
Institut d'Investigacions Biomèdiques August Pi i Sunyer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Portal Hypertension focused on measuring Bleeding gastric varices, Transjugular intrahepatic portosystemic shunt (TIPS), Injection of adhesives

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Hospital Germans Trias i PujolRecruiting
  • ICU Liver Unit. Hospital Clinic of BarcelonaRecruiting
  • Hospital de la Santa Creu i Sant PauRecruiting
  • Hospital del MarRecruiting
  • Hospital Arnau de VilanovaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Early TIPS

Control

Arm Description

Standard treatment to achieve initial hemostasis: vasoactive drugs (somatostatin or terlipressin) + endoscopic injection of tissue adhesives according to the center protocol. Performance of TIPS in the first 5 days following acute gastric variceal bleeding.

Standard treatment to achieve initial hemostasis: vasoactive drugs (somatostatin or terlipressin) + endoscopic injection of tissue adhesives according to the center protocol. Standard combined endoscopic and pharmacological therapy as a secondary prophylaxis (beta-blockers or carvedilol + repeated injection of tissue adhesives until the erradication of the fundal varices).

Outcomes

Primary Outcome Measures

Combined: Absence of rebleeding + survival
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 Outcome Measures

Absence of portal hypertension-related complications (ascites, spontaneous bacterial peritonitis, hepatorenal syndrome)
Comparison of the development of portal-hypertension related complications.
Transfusional requirements
We will compare the number of packed red blood cells required by each treatment arms as a surrogate of rebleeding.
Individual adverse events
Related and not related to the therapies under study.
Hospital stay
Including the stay for the index bleed and also readmissions due to complications of liver disease.
Use of hospital resources
Use of hospital resources other than specified in the treatment arms (TIPS, revision of TIPS patency, derivative surgery or additional endoscopic therapy).

Full Information

First Posted
February 5, 2015
Last Updated
March 13, 2018
Sponsor
Institut d'Investigacions Biomèdiques August Pi i Sunyer
Collaborators
Hospital Clinic of Barcelona, Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, Germans Trias i Pujol Hospital, Hospital Universitario Ramon y Cajal, Hospital del Mar
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1. Study Identification

Unique Protocol Identification Number
NCT02364297
Brief Title
TIPS in Fundal Variceal Bleeding (the TFB Study)
Acronym
TFB
Official Title
Efficacy of Early-TIPS in the Treatment of Acute Variceal Bleeding From Gastric Fundal Varices: a RCT vs Standard Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
November 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut d'Investigacions Biomèdiques August Pi i Sunyer
Collaborators
Hospital Clinic of Barcelona, Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, Germans Trias i Pujol Hospital, Hospital Universitario Ramon y Cajal, Hospital del Mar

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Portal Hypertension, Bleeding Gastric Varices
Keywords
Bleeding gastric varices, Transjugular intrahepatic portosystemic shunt (TIPS), Injection of adhesives

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early TIPS
Arm Type
Active Comparator
Arm Description
Standard treatment to achieve initial hemostasis: vasoactive drugs (somatostatin or terlipressin) + endoscopic injection of tissue adhesives according to the center protocol. Performance of TIPS in the first 5 days following acute gastric variceal bleeding.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Standard treatment to achieve initial hemostasis: vasoactive drugs (somatostatin or terlipressin) + endoscopic injection of tissue adhesives according to the center protocol. Standard combined endoscopic and pharmacological therapy as a secondary prophylaxis (beta-blockers or carvedilol + repeated injection of tissue adhesives until the erradication of the fundal varices).
Intervention Type
Device
Intervention Name(s)
Early TIPS
Intervention Description
TIPS (first 5 days)
Primary Outcome Measure Information:
Title
Combined: Absence of rebleeding + survival
Description
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)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Absence of portal hypertension-related complications (ascites, spontaneous bacterial peritonitis, hepatorenal syndrome)
Description
Comparison of the development of portal-hypertension related complications.
Time Frame
6 weeks and 1 year
Title
Transfusional requirements
Description
We will compare the number of packed red blood cells required by each treatment arms as a surrogate of rebleeding.
Time Frame
6 weeks and 1 year
Title
Individual adverse events
Description
Related and not related to the therapies under study.
Time Frame
1 year
Title
Hospital stay
Description
Including the stay for the index bleed and also readmissions due to complications of liver disease.
Time Frame
1 year
Title
Use of hospital resources
Description
Use of hospital resources other than specified in the treatment arms (TIPS, revision of TIPS patency, derivative surgery or additional endoscopic therapy).
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Angels Escorsell, MD
Phone
34932275400
Ext
4030
Email
aescor@clinic.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angels Escorsell, MD
Organizational Affiliation
Senior Consultant. Liver Unit
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Germans Trias i Pujol
City
Badalona
State/Province
Catalonia
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rosa Morillas, MD
Facility Name
ICU Liver Unit. Hospital Clinic of Barcelona
City
Barcelona
State/Province
Catalonia
ZIP/Postal Code
08036
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angels Escorsell, MD
Phone
34932275400
Ext
4030
Email
aescor@clinic.cat
First Name & Middle Initial & Last Name & Degree
Angels Escorsell, MD
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
State/Province
Catalonia
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Càndid Villanueva, MD
Email
cvillanueva@santpau.cat
Facility Name
Hospital del Mar
City
Barcelona
State/Province
Catalonia
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
José Carrión, MD
Facility Name
Hospital Arnau de Vilanova
City
Lleida
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carles Aracil, MD
Email
carbla34@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
17879356
Citation
Garcia-Tsao G, Sanyal AJ, Grace ND, Carey W; Practice Guidelines Committee of the American Association for the Study of Liver Diseases; Practice Parameters Committee of the American College of Gastroenterology. Prevention and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007 Sep;46(3):922-38. doi: 10.1002/hep.21907. No abstract available. Erratum In: Hepatology. 2007 Dec;46(6):2052.
Results Reference
background
PubMed Identifier
18435460
Citation
Garcia-Tsao G, Bosch J, Groszmann RJ. Portal hypertension and variceal bleeding--unresolved issues. Summary of an American Association for the study of liver diseases and European Association for the study of the liver single-topic conference. Hepatology. 2008 May;47(5):1764-72. doi: 10.1002/hep.22273. No abstract available.
Results Reference
background
PubMed Identifier
20573925
Citation
Garcia-Pagan JC, Caca K, Bureau C, Laleman W, Appenrodt B, Luca A, Abraldes JG, Nevens F, Vinel JP, Mossner J, Bosch J; Early TIPS (Transjugular Intrahepatic Portosystemic Shunt) Cooperative Study Group. Early use of TIPS in patients with cirrhosis and variceal bleeding. N Engl J Med. 2010 Jun 24;362(25):2370-9. doi: 10.1056/NEJMoa0910102.
Results Reference
result

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TIPS in Fundal Variceal Bleeding (the TFB Study)

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