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Endoscopic Cyanoacrylate Obliteration vs. Nadolol Treatment in the Prevention of Gastric Variceal Rebleeding (GVO-nadolol)

Primary Purpose

Liver Cirrhosis and Hepatoma., Gastric Variceal Bleeding

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Nadolol
Sponsored by
Taipei Veterans General Hospital, Taiwan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Liver Cirrhosis and Hepatoma.

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • clinical diagnosis of liver cirrhosis and/or HCC, endoscopically proven gastric variceal bleeding

Exclusion Criteria:

  • younger than 18 y/o or older than 80 y/o, terminal illness, other major systemic disease or malignancy

Sites / Locations

  • Veteran General Hospital-TaipeiRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

G

C

Arm Description

Endoscopic injection of cyanoacrylate alone

Combination of GVO and nadolol

Outcomes

Primary Outcome Measures

Rebleeding

Secondary Outcome Measures

Complication Survival

Full Information

First Posted
December 2, 2007
Last Updated
June 6, 2010
Sponsor
Taipei Veterans General Hospital, Taiwan
Collaborators
National Science Council, Taiwan
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1. Study Identification

Unique Protocol Identification Number
NCT00567216
Brief Title
Endoscopic Cyanoacrylate Obliteration vs. Nadolol Treatment in the Prevention of Gastric Variceal Rebleeding
Acronym
GVO-nadolol
Official Title
A Randomized Tril of Endoscopic Cyanoacrylate Obliteration vs. Nadolol
Study Type
Interventional

2. Study Status

Record Verification Date
June 2010
Overall Recruitment Status
Unknown status
Study Start Date
April 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2010 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Taipei Veterans General Hospital, Taiwan
Collaborators
National Science Council, Taiwan

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Gastric variceal bleeding has a very high rebleeding rate even after endoscopic variceal injection of cyanoacrylate (GVO) which is considered the first choice of endoscopic treatment. Beta-blocker (BB) is effective to lower portal pressure. We hypothesized combination of GVO and BB can further decrease the rebleeding rate.
Detailed Description
Gastric varies (GV) rarely rupture. However should it occur, the outcome would be worse than rupture of esophageal varies (EV). Rupture of GV is characteristic of a higher rebleeding rate, a requirement for a larger amount of blood transfusion and a higher mortality. Up to date, the treatment of GV bleeding (GVB) is still sub-optimal in contrast to the treatment of EV bleeding. The management of GV has been focused on treatment of acute GVB. Various specific methods are used to control GVB and prevent rebleeding; however they were far from ideal. It is because GV are usually larger vessels formed in deeper submucosa and connect to the spontaneous gastrorenal shunt which creates a fast blood flow. Therefore, voluminous blood in the larger diameter GV leads to exsanguine bleeding when ruptured. A variety of endoscopic methods, which include injection of sclerosants, tissue adhesive (cyanoacrylate), thrombin and ligation with rubber bands, detachable nylon loop and steel snares, are applied to control acute GV bleeding with variable successful rates (50~100%) and rebleeding rates (20~90%). The successful rate of endoscopic cyanoacrylate injection to arrest active GVB is more consistent around 90~100% and rebleeding rate is around 30~40%. The recent International Consensus Meeting endorsed that endoscopic cyanoacrylate injection is the first line treatment for acute GVB. The embolic complications, either septic & aseptic, are not uncommon. Expertise is also required to reduce the embolic complications and instrumental injuries. Therefore, the efficacy of specific treatment for GVB is sub-optimal, consecutive innovation of new methods are required to improve the prognosis of GVB. Non-selective beta-blocker is effective to reduce rebleeding from esophageal varices. However, its effect on gastric variceal hemorrhage has never been proven. This is an important issues prompted by current portal hypertension experts. We have much experience in the treatment of gastric variceal bleeding and published fruitful results in high ranking journal. Therefore, we design a randomized trial to compare the effect of endoscopic cyanoacrylate injection obliteration versus non-selective beta-blocker in the secondary prevention of acute gastric variceal bleeding.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis and Hepatoma., Gastric Variceal Bleeding

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
G
Arm Type
No Intervention
Arm Description
Endoscopic injection of cyanoacrylate alone
Arm Title
C
Arm Type
Active Comparator
Arm Description
Combination of GVO and nadolol
Intervention Type
Drug
Intervention Name(s)
Nadolol
Intervention Description
Starting from 20 mg daily, titrated weekly to decrease heart rate more than 25 % of baseline, administrated during the whole study period
Primary Outcome Measure Information:
Title
Rebleeding
Time Frame
3 yr
Secondary Outcome Measure Information:
Title
Complication Survival
Time Frame
3 yr

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: clinical diagnosis of liver cirrhosis and/or HCC, endoscopically proven gastric variceal bleeding Exclusion Criteria: younger than 18 y/o or older than 80 y/o, terminal illness, other major systemic disease or malignancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ming-Chih Hou, MD
Phone
886-2-28712111
Ext
3763
Email
mchou@vghtpe.gov.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Han-Chieh Lin, MD
Phone
886-2-28712111
Ext
3349
Email
hclin@vghtpe.gov.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ming-Chih Hou, MD
Organizational Affiliation
Taipei Veterans General Hospital, Taiwan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Veteran General Hospital-Taipei
City
Taipei city
State/Province
Taiwan
ZIP/Postal Code
11217
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ming-Chih Hou, MD
Phone
886-2-28712111
Ext
3763
Email
mchou@vghtpe.gov.tw
First Name & Middle Initial & Last Name & Degree
Ming-Chih Hou, MD

12. IPD Sharing Statement

Learn more about this trial

Endoscopic Cyanoacrylate Obliteration vs. Nadolol Treatment in the Prevention of Gastric Variceal Rebleeding

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