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Clinical Trials in China / NCT07053605
Recruiting Not applicable

Clinical Study on Laparoscopic Resection of Splenic Artery Aneurysm With Preservation of Spleen

NCT07053605 · tracked via the Priya Life Science China tracker
Sponsor
Northern Jiangsu People's Hospital
Phase
Not applicable
Started
2025-06-23
Last updated
2025-07-08

Condition(s) studied

Splenic Artery AneurysmImmune FunctionHemodynamics

Investigational drug(s) / intervention(s)

laparoscopic resection of splenic artery aneurysm with preservation of spleen

laparoscopic resection of splenic artery aneurysm with preservation of spleen: The laparoscopic resection of splenic artery aneurysm with preservation of spleen is performed by the same surgical team.

Study summary

In this study, researchers examined the changes in related indicators such as immune function, splenic vein,proper hepatic artery, and portal venous hemodynamics following laparoscopic resection of a splenic artery aneurysm. We determined the changes in these patient-related indicators after surgical treatment and whether these changes could improve patient outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Asymptomatic splenic artery aneurysms with a diameter\>2 cm,ruptured splenic artery aneurysms,and splenic artery aneurysms with a diameter increase\>0.5 cm/year. Aneurysm located in the main trunk of the splenic artery. Informed consent to participate in the study. Exclusion Criteria: * Patients with malignancies Hepatic cirrhosis with portal hypertension peptic ulcer disease Recent peptic ulcer disease History of Hemorrhagic stroke Pregnancy hematological diseases Uncontrolled Hypertension Human immunodeficiency virus (HIV) infection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinical Medical College, Yangzhou University Yangzhou Jiangsu Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07053605 on ClinicalTrials.gov ↗ ← All trials in China