Carvedilol as an Adjunct to Endoscopic Cyanoacrylate Injection for Secondary Prophylaxis of Gastric Variceal Bleeding
Primary Purpose
Esophageal and Gastric Varices
Status
Completed
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
carvedilol
cyanoacrylate
Sponsored by

About this trial
This is an interventional treatment trial for Esophageal and Gastric Varices focused on measuring Gastric varices, cyanoacrylate, carvedilol
Eligibility Criteria
Inclusion Criteria:
- Age of 20 to 80 years
- Cirrhotic patients with acute gastric variceal bleeding proven by an endoscopy within 24 h of bleeding
- Stable hemodynamic condition for at least 3 days after cyanoacrylate injection
Exclusion Criteria:
- Previous treatment of gastric varices, including endoscopic therapy, transjugular intrahepatic porto-systemic shunt, or surgery
- Contraindications to non-selective beta-blockers or cyanoacrylate injection
- Serum total bilirubin >10 mg/dL
- Grade III/IV hepatic encephalopathy
- Hepato-renal syndrome
- Severe heart failure (NYHA Fc III/IV)
- Chronic kidney disease under renal replacement therapy
- Refractory ascites
- Malignancy other than hepatocellular carcinoma
- Pregnancy
- Pacemaker use
- Refusal to participate
Sites / Locations
- Kaohsiung Veterans General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cyanoacrylate injection plus carvedilol
Cyanoacrylate injection
Arm Description
The patients undergo repeated endoscopic cyanoacrylate injection every 3-4 weeks until obturation of gastric varices. Oral carvedilol is administrated during the whole study period, starting at 6.25 mg daily and increased until the maximum tolerated dose.
The patients undergo repeated endoscopic cyanoacrylate injection every 3-4 weeks until obturation of gastric varices.
Outcomes
Primary Outcome Measures
Rebleeding From Gastric Varices
Rebleeding from gastric varices during the follow-up period
Secondary Outcome Measures
All Upper Gastrointestinal Bleeding
All upper gastrointestinal bleeding during the follow-up period
All Cause Mortality or Liver Transplantation
All cause mortality or liver transplantation during the study period
All Adverse Effects
All adverse effects during the study period
Full Information
NCT ID
NCT02504723
First Posted
July 18, 2015
Last Updated
July 27, 2017
Sponsor
Kaohsiung Veterans General Hospital.
1. Study Identification
Unique Protocol Identification Number
NCT02504723
Brief Title
Carvedilol as an Adjunct to Endoscopic Cyanoacrylate Injection for Secondary Prophylaxis of Gastric Variceal Bleeding
Official Title
Carvedilol Plus Endoscopic Cyanoacrylate Injection Versus Endoscopic Cyanoacrylate Injection for Secondary Prophylaxis of Gastric Variceal Bleeding
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
December 2011 (Actual)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kaohsiung Veterans General Hospital.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Gastric variceal obturation is the current endoscopic therapy of choice for gastric variceal bleeding but is associated with a high rebleeding rate. Carvedilol is a potent non-selective β-blocker. The role of carvedilol in the prevention of recurrent gastric variceal bleeding is not studied. This study aimed at evaluating the efficacy of carvedilol as an adjunct to gastric variceal obturation in the secondary prophylaxis of gastric variceal bleeding.
Detailed Description
Gastric variceal bleeding is a lethal complication of portal hypertension. The rebleeding rate ranged between 30% to 50% in patients after initial hemostasis. Endoscopic cyanoacrylate injection is currently the choice of endoscopic therapy of acute gastric variceal bleeding and prevention of recurrent bleeding. However, the rebleeding rate is still high in the patients undergoing repeated endoscopic cyanoacrylate injection.
Non-selective β-blockers are frequently used for the secondary prophylaxis of variceal bleeding. In the case of esophageal varices, combination of non-selective β-blockers and endoscopic therapy significantly lowers the rebleeding rate compared with endoscopic therapy alone. However, propranolol failed to decrease the rebleeding rate as an adjunct to endoscopic cyanoacrylate injection and was associated with a higher incidence of adverse effects in gastric variceal bleeding patients. A more potent non-selective β-blocker than propranolol might further decrease portal pressure and decrease the rebleeding rate.
Carvedilol is a potent non-selective β-blocker with both beta and alpha-1 blocker effect. It significantly lowers portal pressure even in propranolol non-responders. However, it is unclear weather carvedilol will play a role in the prevention of recurrent gastric variceal bleeding. The investigators conducted a randomized controlled trial to compare the efficacy of carvedilol combined with endoscopic cyanoacrylate injection with endoscopic cyanoacrylate injection alone in secondary prophylaxis of gastric variceal bleeding.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal and Gastric Varices
Keywords
Gastric varices, cyanoacrylate, carvedilol
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
121 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cyanoacrylate injection plus carvedilol
Arm Type
Experimental
Arm Description
The patients undergo repeated endoscopic cyanoacrylate injection every 3-4 weeks until obturation of gastric varices. Oral carvedilol is administrated during the whole study period, starting at 6.25 mg daily and increased until the maximum tolerated dose.
Arm Title
Cyanoacrylate injection
Arm Type
Active Comparator
Arm Description
The patients undergo repeated endoscopic cyanoacrylate injection every 3-4 weeks until obturation of gastric varices.
Intervention Type
Drug
Intervention Name(s)
carvedilol
Intervention Description
Oral carvedilol is started after randomization at an initial dose of 6.25 mg daily. Doses are increased every 3 days during the admission or every 7 days in the out-patient clinics until the maximum tolerated dose was achieved or up to 25 mg daily, aiming at reducing resting pulse rate by 25 percent but not below 55 beats per minute with systolic blood pressure >90 mm Hg.
Intervention Type
Drug
Intervention Name(s)
cyanoacrylate
Intervention Description
The patients undergo repeated endoscopic cyanoacrylate injection every 3-4 weeks until obturation of gastric varices.
Primary Outcome Measure Information:
Title
Rebleeding From Gastric Varices
Description
Rebleeding from gastric varices during the follow-up period
Time Frame
Within 6 years
Secondary Outcome Measure Information:
Title
All Upper Gastrointestinal Bleeding
Description
All upper gastrointestinal bleeding during the follow-up period
Time Frame
Within 6 years
Title
All Cause Mortality or Liver Transplantation
Description
All cause mortality or liver transplantation during the study period
Time Frame
Within 6 years
Title
All Adverse Effects
Description
All adverse effects during the study period
Time Frame
Within 6 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age of 20 to 80 years
Cirrhotic patients with acute gastric variceal bleeding proven by an endoscopy within 24 h of bleeding
Stable hemodynamic condition for at least 3 days after cyanoacrylate injection
Exclusion Criteria:
Previous treatment of gastric varices, including endoscopic therapy, transjugular intrahepatic porto-systemic shunt, or surgery
Contraindications to non-selective beta-blockers or cyanoacrylate injection
Serum total bilirubin >10 mg/dL
Grade III/IV hepatic encephalopathy
Hepato-renal syndrome
Severe heart failure (NYHA Fc III/IV)
Chronic kidney disease under renal replacement therapy
Refractory ascites
Malignancy other than hepatocellular carcinoma
Pregnancy
Pacemaker use
Refusal to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wen-Chi Chen, MD
Organizational Affiliation
Kaohsiung Veterans General Hospital.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaohsiung Veterans General Hospital
City
Kaohsiung
ZIP/Postal Code
813
Country
Taiwan
12. IPD Sharing Statement
Citations:
PubMed Identifier
30772583
Citation
Chen WC, Hsin IF, Chen PH, Hsu PI, Wang YP, Cheng JS, Lin HS, Hou MC, Lee FY. Addition of Carvedilol to Gastric Variceal Obturation Does Not Decrease Recurrence of Gastric Variceal Bleeding in Patients With Cirrhosis. Clin Gastroenterol Hepatol. 2019 Oct;17(11):2356-2363.e2. doi: 10.1016/j.cgh.2019.02.021. Epub 2019 Feb 14.
Results Reference
derived
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Carvedilol as an Adjunct to Endoscopic Cyanoacrylate Injection for Secondary Prophylaxis of Gastric Variceal Bleeding
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