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Randomized controlled trial of carvedilol and propranolol in the treatment of HVPG patients with cirrhosis and portal hypertension

Randomized controlled trial of carvedilol and propranolol in the treatment of HVPG patients with cirrhosis and portal hypertension

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17012836
Enrollment
Unknown
Registered
2017-09-29
Start date
2017-10-10
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

portal hypertension and cirrhosis

Interventions

Group 1:carvedilol 10mg bid
Group 2:propranolol 60mg bid

Sponsors

Drum Tower Hospital affiliated to Nanjing University Medicine School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old; 2. Tissue biopsy, or at least two imaging examinations, confirmed cirrhosis; 3. Endoscopic confirmation of moderate and severe esophageal and gastric varices; 4. ASevere gastroesophageal varices without bleeding(primary prevention)history of bleeding from esophageal varices or 5 days after acute bleeding (secondary prevention); 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Basal HVPG less than 12 mmHg; 2. The hepatic function of CTP is graded as grade C or severe ascites or severe hepatic failure; 3. Contraindications to ß-blockers, such as bronchial asthma, cardiogenic shock, heart block (II - III degree atrioventricular block), severe or acute heart failure and sinus bradycardia and allergic to this product etc; 4. Patients who takes drugs that affect the metabolism and absorption of non selective beta blockers in vivo; 5. Patients using other drugs that reduce portal pressure; 6. Patients with hepatocellular carcinoma or extrahepatic tumor, portal vein tumor thrombus, or thrombus; 7. Patients with severe heart, lung, liver, and kidney dysfunction, or severe hemorrhagic disease or local / systemic infection, hypothyroidism, Raynaud's syndrome, peripheral vascular disease, etc.; 8. Women who plans to become pregnant or pregnant or nursing.

Design outcomes

Primary

MeasureTime frame
hepatic venous pressure gradient;

Countries

China

Contacts

Public ContactYuzheng Zhuge

Drum Tower Hospital affiliated to Nanjing University Medicine School

yuzheng9111963@aliyun.com+86 15996289206

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 16, 2026