CTRI/2024/05/067972尚未招募2 期
Phase II Study of Spatially Fractionated Radiation Treatment using Rapid Rod Technique for Gynecological Cancers - NI
Varian Medical Systems0 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
- 发起方
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.Patients with cervical cancer post EBRT, with expected suboptimal brachytherapy dose coverage due to-
- •a.Aberrant uterine or pelvic anatomy leading to difficulty in localization of the cervical OS or negotiation of the uterine canal accurately by two independent clinicians in up to two procedures.
- •b.Large residual disease at the time of brachytherapy with anticipated suboptimal target coverage either determined in clinic based on pre-brachytherapy imaging or at dose planning (e.g. figure 3).
- •c.Very narrow vaginal canal not accommodating even the smallest intracavitary or vaginal cylinder applicators.
- •2.Patients with inoperable endometrial cancer not suitable for anaesthesia or have anticipated suboptimal coverage of target volume at brachytherapy as identified on pre-brachytherapy imaging obtained after EBRT.
- •3.Patients with large pelvic recurrences after surgery and/or (chemo) radiation, not amenable to surgical salvage or brachytherapy after salvage EBRT due to reasons specified in item 1.
- •4.Patients with contraindications to anaesthesia for brachytherapy with sufficient risk of on-table or post procedure adverse events.
排除标准
- •1.Any pre-existing fistula in bladder or rectum.
- •2.Pelvic prosthesis.
- •3.Refusal to provide consent.
研究者
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