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临床试验/CTRI/2024/05/067972
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

发起方
Varian Medical Systems

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