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The value of laparoscopic splenectomy as the first-line treatment in secondary prevention of portal hypertensive hemorrhage in cirrhotic patients: a prospective, multicenter, randomized controlled study

Laparoscopic splenectomy as a first-line treatment for secondary prevention of portal hypertension hemorrhage in patients with liver cirrhosis: a prospective, multicenter, randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038306
Enrollment
Unknown
Registered
2020-09-17
Start date
2019-01-01
Completion date
Unknown
Last updated
2020-12-14

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

Conditions

Cirrhotic portal hypertension

Interventions

experimental group:Laparoscopic splenectomy

Sponsors

Shunde Hospital of Southern Medical University (Shunde First People's Hospital, Foshan)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged from 18 to 75 years old, regardless of gender; 2. Patients with liver cirrhosis complicated with portal hypertension diagnosed clinically and / or pathologically; 3. Patients with a history of esophagogastric variceal hemorrhage (melena, hematemesis, etc.) who have never received endoscopic treatment; 4. Patients with HVPG >= 16mmhg were detected after admission; 5. Patients with child Pugh grade A or B; 6. Patients with ECoG score = 60; 7. Patients who voluntarily participated in the study agreed to cooperate with the researchers in data collection and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. Patients with or suspected of liver cancer, cholangiocarcinoma and other malignant tumors; 3. Patients with severe coagulation disorders; 4. Patients with massive ascites; 5. Patients who are not suitable or willing to accept HVPG test; 6. Other situations that the researcher thinks are not suitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
hepatic venous pressure gradient;

Countries

China

Contacts

Public ContactWeidong Wang

Shunde Hospital of Southern Medical University(Shunde First People's Hospital, Foshan)

wangweidong1968@126.com+86 13702835586

Outcome results

None listed

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