Fact CheckerSign in

NCT07811700Completed

Effect of LSD on Lipid Profiles Within 1 Year Postoperatively in Cirrhosis Patients With Portal Hypertension Bleeding

Effect of Laparoscopic Splenectomy and Azygoportal Disconnection on Lipid Profiles Within 1 Year Postoperatively n Cirrhosis Patients With Portal Hypertension Bleeding

Source: ClinicalTrials.gov · Last updated 10 Sept 2026

Brief summary (registry, in English)

Patients with liver cirrhosis frequently exhibit dyslipidemia due to impaired hepatic lipid synthesis, altered bile acid metabolism, and portal hypertension. Laparoscopic Splenectomy and Azygoportal Disconnection (LSD) is commonly used to treat Cirrhosis with Portal Hypertension Bleeding in these patients, but its impact on lipid profiles within 1 year postoperatively remains poorly characterized. This study will follow patients undergoing LSD to measure changes in serum lipid parameters before and after surgery, identify risk factors for lipid profile deterioration or improvement, and determine whether LSD can ameliorate dyslipidemia in the long term, thereby informing metabolic management strategies in cirrhotic patients.

Status (registry)
Completed
Study type
Observational
Enrollment
150 (actual)
First submitted
3 Sept 2026
Start date
1 May 2022
Primary completion date
1 May 2025
Lead sponsor
Northern Jiangsu People's Hospital
NCT number
NCT07811700

What you commit to

  • Study type: Observational
  • Participants enrolled: 150
  • From 1 May 2022 to the primary completion date, 1 May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous abdominal surgery precluding safe laparoscopic splenectomy and azygoportal disconnection
  • Metabolic/endocrine diseases: Familial hyperlipidemia; uncontrolled severe diabetes mellitus, thyroid dysfunction, nephrotic syndrome; use of lipid-lowering drugs, hormones, or other drugs affecting blood lipids within 1 month before surgery.
  • Cirrhotic complications (hepatic encephalopathy, refractory ascites) within 1 month before surgery

Other illness

  • Severe cardiac, pulmonary, cerebrovascular dysfunction; malignant tumors; primary hematological disorders
  • Infections/inflammatory diseases: Active hepatitis, severe infections, or autoimmune diseases.

Other

  • Child-Pugh Class C liver cirrhosis
  • Pregnancy or lactation
  • Poor compliance, inability to complete follow-up

Who the study is looking for

  • Age 18-80 years, male or female
  • Confirmed diagnosis of liver cirrhosis (clinical, laboratory, imaging)
  • Splenomegaly and hypersplenism
  • History of portal hypertension bleeding (esophageal and gastric variceal bleeding )
  • Child-Pugh Class A or B liver function
  • Ability to complete 12-month follow-up

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinical Medical College of Yangzhou University
Coordinator of this site? Confirm its status
YangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.