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Carvedilol tablets compared with endoscopic banding treatment in preventing rebleeding from oesophgaeal varices

Multicentre randomised controlled study comparing carvedilol with endoscopic band ligation in the prevention of variceal rebleeding

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN69643049
Enrollment
152
Registered
2013-12-06
Start date
2006-06-06
Completion date
Unknown
Last updated
2016-11-28

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

Conditions

Variceal rebleeding in cirrhotic patients Digestive System Other diseases of liver

Interventions

Oral carvedilol tablets versus endoscopic band ligation Carvedilol is 6.25 mg once daily for one week and if tolerated then 12.5 mg once daily until the study is completed (6 months after the last pa

Sponsors

Greater Glasgow & Clyde (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male or female aged =18 and <75yrs 2. Endoscopic diagnosis of oesophageal variceal bleeding 3. Cirrhosis (based on previous liver biopsy or clinical, biochemical and ultrasonographic findings)

Exclusion criteria

Exclusion criteria: 1. Age 75 years 2. Advanced malignancy or another condition associated with a life expectancy of < 6/12 months 3. Previous transjugular intrahepatic portosystemic shunt (TIPS) or porto-caval shunt surgery 4. Portal vein thrombosis 5. Obstructive airways disease 6. Severe peripheral vascular disease 7. Heart block 8. Severe heart failure 9. Pregnancy 10. Type I diabetes mellitus 11. Gastric variceal bleed 12. Treatment with beta blockers or alpha blockers within 4 weeks of index bleed

Design outcomes

Primary

MeasureTime frame
Variceal rebleeding is monitored when it occurs during follow-up. Patients will be followed up until 6 months after the last patient is randomised.

Secondary

MeasureTime frame
1. Mortality 2. Any upper gastointestinal bleeding is monitored when it occurs during follow-up

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026