跳至主要内容
临床试验/ISRCTN84013636
ISRCTN84013636已完成3 期

PHOTOdynamic versus white light-guided treatment of non-muscle invasive bladder cancer: randomised trial of clinical and cost-effectiveness

ewcastle upon Tyne Hospitals NHS Foundation Trust (UK)0 个研究点目标入组 538 人开始时间: 2014年7月25日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
538

研究概览

简要总结

2019 Protocol article in https://pubmed.ncbi.nlm.nih.gov/31481549/ protocol (added 05/10/2020) 2022 Results article in https://doi.org/10.1056/EVIDoa2200092 (added 27/09/2022) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36300825/ (added 28/10/2022)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Adult men and women aged = 16 years
  • 2. First suspected diagnosis of bladder cancer
  • 3. Visual/ultrasound/CT diagnosis of intermediate/high risk NMIBC
  • 3.1. White light visual appearances of intermediate or high risk disease (=> 3cm, two or more tumours, or flat velvety erythematous changes alerting a clinical suspicion of CIS).
  • 3.2. Suspicion of papillary bladder tumour > 3cm based on ultrasound or computerized tomography (CT) scanning (without hydronephrosis)
  • 4. Written informed consent for participation prior to any study specific procedures
  • 5. Willing to comply with lifestyle guidelines

排除标准

  • 1. Visual evidence of low risk NMIBC (solitary tumour < 3cm)
  • 2. Visual evidence of MIBC on preliminary cystoscopy, i.e. nonpapillary or sessile mass (attached directly by its base without a stalk)
  • 3. Imaging evidence of MIBC CT/USS (this includes the presence of hydronephrosis, which may be present despite clear imaging of MIBC in the bladder)
  • 4. Upper tract (kidney or ureteric) tumours on imaging
  • 5. Any other malignancy in the past 2 years (except: nonmelanomatous skin cancer cured by excision, adequately treated carcinoma in situ of the cervix, DCIS/LCIS of the breast or prostate cancer in patients who have a life expectancy of >5 years upon trial entry)
  • 6. Evidence of metastases
  • 7. Porphyria or known hypersensitivity to porphyrins
  • 8. Known pregnancy (based on history and without formal testing, in keeping with day-to-day NHS practice of PDD use)
  • 9. Any other conditions that in the Principal Investigator?s opinion would contraindicate protocol treatment
  • 10. Unable to provide informed consent
  • 11. Unable or unwilling to complete follow up schedule (including questionnaires)

研究者

发起方
ewcastle upon Tyne Hospitals NHS Foundation Trust (UK)

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