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Comparison of effects of carvedilol and PSE on HVPG: a prospective multicenter randomized controlled trial

Comparison of effects of carvedilol and PSE on HVPG: a prospective multicenter randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027380
Enrollment
Unknown
Registered
2019-11-11
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

Cirrhotic portal hypertension

Interventions

A:Oral carvedilol
B:PSE

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed as cirrhosis, including pathological diagnosis or clinical and imaging confirmation; 2. Endoscopy confirmed the presence of esophageal and gastric varices; 3. HVPG >= 10mmHg; 4. Aged between 18 and 75 years; 5. Have good compliance with the proposed treatment requirements; 6. Obtain the subject's informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of rupture of esophagogastric varices; 2. Esophageal varices have included endoscopic treatment, NSBB, TIPS or surgical treatment; 3. Carvedilol or PSE contraindications; 4. Confirm malignant tumors including hepatocellular carcinoma or other diseases that will shorten the lifespan of patients; 5. Cardiopulmonary failure; 6. The subject refuses to participate in the trial or does not have the ability to sign informed consent; 7. Pregnant or lactating women; 8. Researchers believe that poor compliance.

Design outcomes

Primary

MeasureTime frame
HVPG;Bleeding rate;

Countries

China

Contacts

Public ContactChunqing Zhang

Shandong Provincial Hospital

zhangchunqing_sdu@163.com+86 13583188661

Outcome results

None listed

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