This study assesses the effectiveness of microwave ablation of the spleen in conjunction with splenic artery occlusion for treating secondary hypersplenism.
Eligibility
Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria:
* 1\. written informed consent signed prior to enrolment 2. age \> 18 years, both sexes 3.Patients with severe hypersplenism secondary to cirrhosis with clinical diagnosis, White blood cells \<3×109/L, and/or platelet \<50×109/L 4.Patients who have been repeatedly given drugs to raise white blood cells and platelets in clinical practice have poor effect 5.Mental problems such as clinical symptoms or anxiety in patients require interventional treatment for hypersplenism
Exclusion Criteria:
* Patients with any of the following are not eligible for enrollment in this study
1. Coagulopathy or other blood disorders
2. Recent use of anticoagulant drugs
3. Severe hypertension and cardiac insufficiency
4. Bone marrow aspiration results showed bone marrow suppression
5. Combined with other spleen malignant diseases
6. Severe skin infection at the puncture site
7. Participated in other clinical studies within 2 months prior to the start of the study
8. Patient or his/her authorized person is unwilling to sign a written informed consent form or unwilling to comply with the study protocol
Primary outcome measure(s)
Dynamic changes in platelet and white blood cell counts in routine blood tests — Up to 1 year Platelet and WBC count changes on CBC
Hepatic artery blood flow velocity — Up to 1 year Hepatic artery blood flow velocity
Routine blood test — Up to 1 year Platelet count
Adverse Events — Up to 1 year Adverse Events
Trial sites (1)
Facility
City
Region
Status
Tianjin Medical University Cancer Institute & Hospital
Tianjin
Tianjin Municipality
Recruiting
More Tianjin Medical University Cancer Institute and Hospital trials in China
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.
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