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临床试验/EUCTR2007-001581-32-GB
EUCTR2007-001581-32-GB进行中(未招募)1 期

Phase I trial of photodynamic therapy using systemic 5-aminolaevulinic acid for the treatment of grade 3 anal intraepithelial neoplasia. - PDT using ALA for the treatment of Grade 3 AI

Joint UCLH & UCL Biomedical Research Unit0 个研究点目标入组 12 人开始时间: 2007年5月16日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Patients with biopsy-proven grade 3 AIN of the anal canal, with or without involvement of the perianal skin, with no evidence of invasive cancer.
  • 2. Males and non-pregnant females over the age of 18 years. Female patients who are pre-menopausal must practice a medically acceptable form of contraception.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Presence of invasive carcinoma of the anus.
  • 2. History of severe cardiovascular disease, severe angina, congestive heart failure, or recent syncope of cardiovascular origin.
  • 3. Patients presenting with abnormal cardiac signs or symtoms and signs of congestive heart failure on physical examination.
  • 4. Patients with orthostatic hypotension resistant to hydration.
  • 5. Patients who have a history of porphyria, or hypersensitivity to porphyrins.
  • 6. Patients taking depot preparations of psychotropic medication.
  • 7. Patients with a white cell count < 2x10e9/L.
  • 8. Patients with a CD4 count < 200 cells/cubic mm.
  • 9. Patients with a platelet count < 50x10e9/L.
  • 10. Patients with a prothrombin time of > 1.5 times the upper limit of normal.
  • 11. Patients with impaired renal and/or hepatic function at the time of entry into the study.
  • 12. Patients receiving concurrent chemotherapy, or radiation therapy or chemotherapy within 4 weeks of entry into the study.

研究者

发起方
Joint UCLH & UCL Biomedical Research Unit

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