ITMCTR2000003631Not yet recruitingPhase 1
A randomized controlled clinical study of anti-cancer decoction no.2 combined with high intensity focused ultrasound in treating primary hepatic carcinoma
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Ages
- 18 to 75 (—)
- Sex
- All
Inclusion Criteria
- •(1) Meet the clinical or (and) pathological diagnostic criteria for primary hepatic cancer;
- •(2) Intermediate and advanced primary hepatic cancer without surgical indications;
- •(3) Measurable primary lesion confirmed by CT or MRI imaging examination;
- •(4) The patient's physical condition was good, with the physical condition score (Karnofsky) >= 60;
- •(5) The expected survival time is more than 3 months;
- •(6) The functions of all organs are basically normal;
- •(7) Child-pugh A and B in liver function;
- •(8) All the surgeries, radiotherapy, TACE and other treatments have been completed for more than 3 months, and all the adverse reactions have recovered after treatment;
- •(9) Patients with obstructive jaundice must be treated with ERCP biliary stent drainage;
- •(10) Voluntarily accept high energy focused ultrasound (HIFU) treatment and sign a written agreement with good compliance.
Exclusion Criteria
- •(1) There is skin rupture or infection in the ultrasound treatment channel;
- •(2) Complicated with other serious basic diseases such as heart, lung and kidney failure;
- •(3) Severe coagulation dysfunction or clear bleeding tendency;
- •(4) Patients with moderate or above ascites;
- •(5) Obvious calcified plaque exists in the arterial wall of the ultrasound treatment channel;
- •(6) Previous severe psychological or mental abnormalities, and estimated insufficient compliance to participate in this study.
Investigators
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