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A prospective study to evaluate the long-term effect of carvedilol versus propranolol on reduction in portal pressure in cirrhotic patients

Not Applicable
Recruiting
Conditions
Diseases of the digestive system
Registration Number
KCT0000102
Lead Sponsor
Hanyang University Guri Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
130
Inclusion Criteria

(1) cirrhosis
(2) severe portal hypertension (hepatic venous pressure gradient > 12mmHg)
(3) F2/F3 varices or endoscopic treatment of large esophageal varices at least 3 months old the last time
(4) Child-Pugh score < 12
(5) not taking patients beta-blocker, ACE inhibitor, nitrate within 1 month

Exclusion Criteria

(1) systolic blood pressure < 90 mmHg, baseline heart rate < 55/min
(2) refractory ascites, hepatic encephalopathy, hepatorenal syndrome
(3) hepatocellular carcinoma
(4) presence of severe systemic illness
(5) history of gastric variceal hemorrhage
(6) contraindication of beta-blocker
(7) serum jaundice > 10 mg/dL
(8) srum creatinine = 1.2 mg/dL
(9) history of shunt or TIPS
(10) IDDM
(11) pregnancy
(12) allergy to beta-blocker or alpha-blocker
(13) unwilling to sign inform consent
(14) Clinical investigator have determined that patient is difficult to perform the clinical trial.

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
reduction of hepatic pressure gradient
Secondary Outcome Measures
NameTimeMethod
compliance;incidence of variceal bleeding;the relationship between hepatic venous pressure gradinet and ultrasonographic findings
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