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临床试验/ISRCTN46587767
ISRCTN46587767已完成未知

A pilot study to optimise the use of FDG PET-CT and deformable image co-registration for lymphoma radiotherapy planning

eeds Teaching Hospitals NHS Trust0 个研究点目标入组 19 人开始时间: 2016年6月28日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
19

研究概览

简要总结

2018 Results article in https://pubmed.ncbi.nlm.nih.gov/30246160/ (added 10/07/2023)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Age =18 years
  • 2. WHO Performance status 0-2 (Appendix A)
  • 3. Histologically proven Hodgkin lymphoma or high grade non-Hodgkin lymphoma
  • 4. Ann Arbor Stage I/II disease based upon clinical examination and any radiology investigations performed
  • 5. Clinical decision to proceed with sequential chemotherapy and radiotherapy if stage I/II disease is confirmed on subsequent PET-CT staging
  • 6. Residual disease in situ after biopsy (either palpable or on any imaging acquired pre-PET-CT)
  • 7. Able to provide fully informed written consent
  • 8. Able to lie flat for 1 hour
  • 9. Not be pregnant or breast feeding. Female patients of childbearing potential must agree to use effective contraception, be surgically sterile, or be post-menopausal

排除标准

  • 1. Hypersensitivity to 18Fluorine-FDG
  • 2. Hypersensitivity to iodinated contrast media
  • 3. Poorly controlled diabetes
  • 4. Acute renal failure or moderate renal impairment (estimated glomerular filtration rate < 30 mL/min)
  • 5. Uncontrolled pain
  • 6. Urinary incontinence
  • 7. Female patients must not be pregnant and if of child bearing age using adequate contraception
  • 8. Breast feeding
  • 9. Serious psychiatric comorbidity

研究者

发起方
eeds Teaching Hospitals NHS Trust

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