Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT05421507

3D-PCT Combined With CT-guided Radioactive I-125 Seed Implantation in the Treatment of Head and Neck Tumors

Led by Peking University Third Hospital · Updated on 2022-07-20

30

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to verify the accuracy, short-term efficacy and side effects of 3D printing coplanar template combined with CT-guided I-125 seeds implantation in the treatment of malignant tumors of the head and neck.

CONDITIONS

Official Title

3D-PCT Combined With CT-guided Radioactive I-125 Seed Implantation in the Treatment of Head and Neck Tumors

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years
  • Clear pathological diagnosis of head and neck tumor with local recurrence or metastasis after surgery or radiotherapy
  • Tumor diameter 5 cm or less, with up to 3 lesions
  • Suitable puncture path available to reach prescribed target dose
  • Karnofsky Performance Status (KPS) score of 70 or higher
  • Expected survival time longer than 3 months
  • Signed consent for I-125 seed implantation therapy
  • Signed consent to participate in this observational study
Not Eligible

You will not qualify if you...

  • Coagulation dysfunction
  • Tumor surface rupture or extensive tumor liquefaction and necrosis causing poor seed distribution
  • Severe underlying diseases making seed implantation unsafe, including active infections requiring treatment
  • Mental abnormalities affecting cognitive ability
  • Poor compliance or inability to complete treatment
  • Considered unsuitable to participate in this clinical trial

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

Department of Radiation Oncology of Peking university third hospital

Beijing, China

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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