CTRI/2017/03/008172尚未招募1 期
A feasibility and safety study of single application multi-fractionated high dose rate (HDR) brachytherapy in locally advanced cervical cancer
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 入组人数
- 40
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) Histologically diagnosed invasive cervical cancer (squamous carcinoma, adenosquamous carcinoma, adenocarcinoma)
- •2) FIGO stage II B - IV A after thorough clinical examination and work-up investigation.
- •3) Suitable for radical radiation therapy with/without chemotherapy, and also for brachytherapy boost.
- •4)Accepts the Informed consent process and signs the form on his/her will.
排除标准
- •1)Patients with vesico-vaginal fistula or recto-vaginal fistula at diagnosis.
- •2)Patients at high risk of anaesthesia and patients with phobia /contra-indications to undergo MRI.
- •3)Patients not suitable for brachytherapy.
- •4)Metastatic disease beyond iliac on standard imaging.
- •5)Vault cancers/recurrence.
- •6)Previous history of pelvic radiation.
- •7)Non-compliance to treatment.
- •8)Medical or psychological illness precluding treatment protocol
研究者
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