Hypertension Clinical Trial
— SVELOfficial title:
Vagus Nerve-preserving Laparoscopic Splenectomy and Azygoportal Disconnection With Versus Without Intraoperative Endoscopic Variceal Ligation
Verified date | December 2023 |
Source | Northern Jiangsu People's Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aimed to evaluate whether synchronous vagus nerve-preserving laparoscopic splenectomy and azygoportal disconnection with intraoperative endoscopic variceal ligation (SVEL) is effective and safe, and to determine whether SVEL can effectively decrease the incidence of postoperative esophageal variceal re-bleeding.
Status | Completed |
Enrollment | 88 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - A clinical, radiological or histologic diagnosis of cirrhosis of any etiology - Splenomegaly with secondary hypersplenism - esophageal/gastroesophageal variceal bleeding - No evidence of portal vein system thrombosis by ultrasound evaluation and angio-CT - Informed consent to participate in the study Exclusion Criteria: - Hepatocellular carcinoma or any other malignancy, - Hypercoagulable state other than the liver disease related - DRUGS- oral contraceptives, anticoagulation or anti-platelet drugs. - Child - Pugh C - Recent peptic ulcer disease - History of Hemorrhagic stroke - Pregnancy - Uncontrolled Hypertension - Age>75 yrs - Human immunodeficiency virus (HIV) infection |
Country | Name | City | State |
---|---|---|---|
China | Clinical Medical College, Yangzhou University | Yangzhou | Jiangsu |
Lead Sponsor | Collaborator |
---|---|
Northern Jiangsu People's Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Esophageal variceal re-bleeding | Proportions of patients who will suffer from esophageal variceal re-bleeding | 1 year | |
Secondary | Death due to re-bleeding | Proportions of patients who will suffer from death due to re-bleeding | 1 year | |
Secondary | Overall survival | Overall survival in both groups | 1 year |
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