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临床试验/CTRI/2022/11/047794
CTRI/2022/11/047794尚未招募2 期

Capecitabine- Based Chemoradiotherapy for Cisplatin ineligible Squamous Cell Carcinoma of the Uterine Cervix

Cancer Institute WIA0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Untreated squamous cell carcinoma of cervix who are planned for definitive
  • chemoradiation
  • 2. Cisplatin ineligible â?? Sensorineural hearing loss, Sensory/Motor neuropathy
  • > grade 2, Borderline renal dysfunction (Calculated creatinine clearance > 30
  • - 60ml/min), or patientâ??s unwillingness to receive cisplatin/intravenous
  • chemotherapy.
  • 3. Eastern Cooperative Oncology Group performance status of 0, 1, or 2.
  • 4. Adequate Aspartate transaminase (AST) and Alanine transaminase (ALT)
  • within 3 times the upper limit of normal (ULN), serum bilirubin less than 2

排除标准

  • 1. Preexisting coronary heart disease (Unstable angina, Echocardiography
  • showing regional wall motion abnormalities or ejection fraction < 50 %),
  • NYHA (Newyork Heart Association) class > 2
  • 2. Known dihydropyramidine dehydrogenase (DPD) mutation
  • 3. Creatinine clearance < 30ml/min
  • 4. Uncontrolled comorbid illness
  • 5. Inflammatory bowel disease
  • 6. Patient taking oral anti coagulants like warfarin

研究者

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