Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06292715

Microwave Ablation With Splenic Artery Occlusion for Secondary Hypersplenism

Led by Tianjin Medical University Cancer Institute and Hospital · Updated on 2024-03-05

35

Participants Needed

1

Research Sites

153 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study assesses the effectiveness of microwave ablation of the spleen in conjunction with splenic artery occlusion for treating secondary hypersplenism.

CONDITIONS

Official Title

Microwave Ablation With Splenic Artery Occlusion for Secondary Hypersplenism

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed written informed consent before joining the study
  • Age over 18 years, any gender
  • Severe secondary hypersplenism caused by cirrhosis with clinical diagnosis
  • White blood cell count less than 3 x 10⁹/L and/or platelet count less than 50 x 10⁹/L
  • Poor response to repeated drug treatments aimed at raising white blood cells and platelets
  • Mental or clinical symptoms such as anxiety requiring interventional treatment for hypersplenism
Not Eligible

You will not qualify if you...

  • Presence of blood clotting problems or other blood disorders
  • Recent use of anticoagulant medications
  • Severe high blood pressure or heart failure
  • Bone marrow suppression shown by bone marrow aspiration
  • Other malignant diseases affecting the spleen
  • Severe skin infection at the site where puncture would occur
  • Participation in another clinical study within 2 months before this study
  • Unwillingness to sign informed consent or follow the study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tianjin Medical University Cancer Institute & Hospital

Tianjin, Tianjin Municipality, China, 300060

Actively Recruiting

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Research Team

W

WEI LU, PhD

CONTACT

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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