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临床试验/EUCTR2006-005795-41-IT
EUCTR2006-005795-41-IT进行中(未招募)1 期

A CLINICO-PATHOLOGICAL PHASE II STUDY WITH TRANSLATIONAL ELEMENTS TOINVESTIGATE THE POSSIBLE INFECTIVE CAUSES OF NON-HODGKIN LYMPHOMA OF THE OCULAR ADNEXAE WITH PARTICULAR REFERENCE TO CHLAMYDIA SPECIES AND THE EFFECTS OF MALT LYMPHOMA TREATMENT WITH TETRACYCLINE - ND

INTERNATIONAL EXTRANODAL LYMPHOMA STUDY GROUP (IELSG)0 个研究点目标入组 100 人开始时间: 2007年6月11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
100

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. Age 16 years or over
  • 2. Histologically confirmed marginal zone B-cell lymphoma of MALT-type
  • 3. Lymphoma localised to the ocular adnexae (conjunctiva, lacrymal gland, orbit soft tissue, clinical stage IEA) 4. No previous treatment, excepting RT for localised lymphoma of the contralateral eye
  • 5. At least one measurable lesion
  • 6. No systemic antibiotic therapy in the last three months
  • 7. No other malignancy in the previous 5 years apart from appropriately treated basal cell carcinoma of the skin or carcinoma in situ of the cervix
  • 8. In women with reproductive potential a willingness to use contraception from entry
  • into the study for a period of 3 months
  • 9. Written informed consent
  • Are the trial subjects under 18? yes
  • 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. Pregnant or lactating women
  • 2. Known allergy to tetracycline
  • 3. Patients unwilling to comply with the requirements of follow-up as defined by this protocol
  • 4. Myasthenia gravis (tetracycline can exacerbate muscle weakness)
  • 5. Systemic lupus erythematous (tetracycline can exacerbate the condition)
  • 6. Patients with large or rapidly enlarging tumours requiring immediate radiotherapy

研究者

发起方
INTERNATIONAL EXTRANODAL LYMPHOMA STUDY GROUP (IELSG)

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