Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07053605

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

Led by Northern Jiangsu People's Hospital · Updated on 2025-07-08

10

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates patients with splenic artery aneurysm, focusing on changes in immune function and blood flow dynamics in the splenic vein, proper hepatic artery, and portal vein after laparoscopic surgery. The study aims to understand how these changes relate to patient outcomes following the surgical removal of the aneurysm while preserving the spleen. Participants undergo laparoscopic resection of the splenic artery aneurysm performed by the same surgical team. After surgery, they receive standardized care and follow a postoperative treatment plan that includes medications and other therapies. Patients are monitored through blood tests and imaging to evaluate immune function and blood flow at multiple times: before surgery and at 7 days, 1 month, 3 months, 6 months, and 12 months after the operation. During the study, participants will have routine blood tests measuring various blood components and immune markers, as well as assessments of blood vessel diameter and flow velocity. Researchers will also monitor for thrombosis in the portal venous system throughout the first year. Follow-up visits and evaluations will allow tracking of recovery and treatment effects over a full year from surgery.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Asymptomatic splenic artery aneurysms larger than 2 cm, ruptured aneurysms, or aneurysms growing more than 0.5 cm per year
  • Aneurysm located in the main trunk of the splenic artery
  • Informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Patients with malignancies
  • Hepatic cirrhosis with portal hypertension
  • Recent peptic ulcer disease
  • History of hemorrhagic stroke
  • Pregnancy
  • Hematological diseases
  • Uncontrolled hypertension
  • Human immunodeficiency virus (HIV) infection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 1 week or until discharge

Participants undergo laparoscopic resection of the splenic artery aneurysm with preservation of the spleen, followed by standardized post-operative care provided by the nursing team.

1 surgical procedure and hospitalization period

Post-operative Follow-up

Duration - 12 months

Participants receive standardized post-operative treatment including pharmacotherapy and additional therapeutic interventions. Routine blood tests, liver function tests, coagulation function, immune function, and hemodynamics of the portal vein, proper hepatic artery, and splenic vein are monitored at multiple time points.

Follow-up visits at 7 days, 1 month, 3 months, 6 months, and 12 months post-surgery

Trial Site Locations

Total: 1 location

1

Clinical Medical College, Yangzhou University

Yangzhou, Jiangsu, China, China

Actively Recruiting

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Research Team

G

Guo-Qing Jiang

D

Dou-Sheng Bai

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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