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临床试验/NCT03609528
NCT03609528已完成不适用

CamPROBE: Developing a Safer and Simple Device for Local Anaesthetic Transperineal Prostate Biopsies

Cambridge University Hospitals NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年2月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Incidence of Infection

研究概览

简要总结

The CamPROBE study investigates the rate of infective complications using the Cambridge Prostate Biopsy Device method of local anaesthetic transperineal prostate biopsies.

详细描述

The current method for diagnosing prostate cancer requires a biopsy needle to pass through the bowel wall to reach the prostate. Bacteria in the bowel inevitably enter the urinary system and blood stream. A significant number of men develop infections despite preventative antibiotics (1 in 10 develop fevers/shivers and 1-2 in 100 get a life-threatening infection). It is crucial we find a safer biopsy method for suspected prostate cancer as over 1 million rectal biopsies occur each year.

A safer alternative device was developed, performed under local anaesthetic using the transperineal route: CamPROBE (Cambridge Prostate Biopsy Device). CamPROBE biopsies are taken through the perineum (the area under the testicles), so there is no infection risk, and it's just as good at diagnosing prostate cancer. This investigation progresses from a prototype to a disposable, single use device that any UK hospital can use. The study will assess CamPROBE's ability to reduce infections from prostate biopsies and its usability as an alternative to the current standard biopsies.

Men recommended to undergo a prostate biopsy will be eligible for this multi-centre study. For each patient, the study will take approximately 30 days, consisting of: recruitment, 1 day for the procedure (replaces the standard biopsy pathway) and questionnaires on day 1, 7 and 30. This timeframe will not introduce delays in the patients' normal standard care pathway. Patients will have a transperineal biopsy with CamPROBE instead of the current transrectal method. Biopsy samples will be treated the same as standard procedure. Patients' acceptability of the procedure and complications will be measured using patient self-reported questionnaires.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • To be included in the clinical investigation the participant must:
  • Have given written informed consent to participate
  • Be aged 18 years and over
  • Be suitable for a prostate biopsy and clinically due to have a biopsy for diagnostic or surveillance purposes
  • Be willing and able to comply with scheduled visits and completion of study questionnaires

排除标准

  • The presence of any of the following will preclude participant inclusion:
  • Contraindication to a prostate biopsy
  • Previous perineal or anal surgery
  • Unable to lie down with legs in a stirrup for at least 45 minutes, as assessed by a clinician

结局指标

主要结局

Incidence of Infection

时间窗: 30 days post biopsy

Changes in incidence of infection as measured using patient self-reported Follow-Up Questionnaires and telephone assessments.

次要结局

  • Patient reported pain score(30 days post biopsy)
  • Patient willingness to have a repeat biopsy(30 days post biopsy)
  • Biological functions post biopsy(30 days post biopsy)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vincent Gnanapragasam

Mr

Cambridge University Hospitals NHS Foundation Trust

研究点 (2)

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