Actively Recruiting
Accuracy of Coplanar Template Assisted Seed Implantation for Abdominal and Pelvic Cancer
Led by Peking University Third Hospital · Updated on 2024-06-18
34
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In recent years, template guidance has been applied and developed in the field of puncture related operations, such as template-assisted radioactive seed implantation. With the guidance of template, needle pathway of seed implantation, biopsy and fiducial marker implantation can be precisely planned actual operation, which is conducive to the accurate proceeding. Templates can be divided into coplanar templates and non-coplanar templates. The digital coplanar template coordinate puncture system has been developed in China and has been applied in clinical practice. In previous studies, coplanar template assisted CT-guided radioactive seed implantation has good clinical feasibility for head and neck cancer. However, the accuracy of Coplanar Template Assisted Seed Implantation for Abdominal and Pelvic cancer are lacking in prospective studies. The study aims to prospectively observe the accuracy and safety of Coplanar Template Assisted Seed Implantation for Abdominal and Pelvic cancer.
CONDITIONS
Official Title
Accuracy of Coplanar Template Assisted Seed Implantation for Abdominal and Pelvic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ages 18 to 85
- Single or multiple abdominal or pelvic tumors (solid, partially solid)
- Not currently taking drugs that affect coagulation or platelet aggregation, or such drugs have been stopped for a sufficient period (e.g., 1 week)
- Karnofsky Performance Status (KPS) greater than 60 with expected survival over 3 months, no serious or uncontrolled underlying diseases, and able to tolerate puncture
- Planned seed implantation with an applicable puncture path
- Provided informed consent
You will not qualify if you...
- Poor organ function such as liver decompensation
- Tumors close to blood vessels or intestines, or presence of portal vein hypertension or superior vena cava compression increasing risk of bleeding or intestinal injury
- Poor compliance or inability to complete required study coordination
- Considered inappropriate or unwilling to participate for other reasons
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Peking University Third Hospital
Beijing, Beijing Municipality, China
Actively Recruiting
Research Team
B
Bin Qiu, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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