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临床试验/NCT03859804
NCT03859804已完成不适用

Comparison of Pain Levels in Fusion Prostate Biopsy and Standard TRUS-Guided Biopsy

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 252 人开始时间: 2016年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
252
试验地点
1
主要终点
Over all Visual analogue Score (VAS) score of procedure(From 0 to 100 points, 100 is max pain score according to patient)

研究概览

简要总结

The aim of this study was to compare the pain levels in transrectal ultrasound (TRUS)-guided standard 12-core prostate biopsy (SPB) and multiparametric prostate magnetic resonance imaging (MpMRI)-guided fusion prostate biopsy (FPB).

详细描述

The study included patients that underwent prostate biopsy under local anesthesia (intrarectal 2% lidocaine gel + periprostatic nerve block) due to suspected prostate cancer. Patients detected with a Prostate Imaging Reporting and Data System score (PIRADS) ≥3 lesion on MpMRI underwent MpMRI-guided FPB (Group I) and the patients who had no suspected lesions or had a PI-RADS <3 lesion on MpMRI underwent TRUS-guided SPB (Group II). Pain assessment was performed using Visual Analog Scale (VAS) 5 min after the procedure. Following the procedure, the patients were asked to indicate the most painful biopsy step among the three steps (1: insertion of the probe into the rectum, 2: probe manipulation, 3: the piercing of the biopsy needle).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Elevated blood prostate specific antigen (PSA) levels according to patients age. PSA >2ng/ml for whom aged between 50-60, and PSA >4ng/ml for whom were above 60 years old
  • •Having suspicious digital rectal examination
  • •having multi-parametric prostate MRI before prostate biopsy
  • •Having MRI defined lesions which were PIRADS - 3 -4-5

排除标准

  • •PSA > 50 ng/ml
  • •previous negative biopsy
  • •neurological disorders that could affect the pain level such as paraplegia or hemiplegia, analgesics use for any reason on the day of or the day before the procedure,
  • •patients underwent biopsy under general anesthesia,
  • •having such diseases as anal fissure or hemorrhoidal disease that could alter the pain threshold

研究组 & 干预措施

Group 1

Experimental

In Group 1, Patients detected with a PI-RADS (Prostate Imaging Reporting and Data System) ≥3 lesion on MpMRI underwent MpMRI-guided MRI- US fusion prostate biopsy. In this fusion biopsy, 12 core standard biopsy and 2-4 cores of biopsies from lesions defined on multiparametric prostate MRI

干预措施: MRI- US fusion prostate biopsy (FPB) (Procedure)

Group 2

Active Comparator

In Group 2, patients who had no suspected lesions or had a PI-RADS <3 lesion on MpMRI underwent Transrectal ultrasound guided 12 core prostate biopsy (SPB).

干预措施: Standard transrectal 12 core biopsy (Procedure)

结局指标

主要结局

Over all Visual analogue Score (VAS) score of procedure(From 0 to 100 points, 100 is max pain score according to patient)

时间窗: Within 5 minutes after prostate biopsy

pain assessment was performed using Visual Analogue Scale (VAS)

To detect painful steps of biopsy procedure by asking patients verbally

时间窗: Within 5 minutes after biopsy

to ask patients most painful step of procedure that verbally defined them before biopsy as 1: insertion of the probe into the rectum, 2: probe manipulation, and 3: the piercing of the biopsy needle

次要结局

未报告次要终点

研究者

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

Abdullah Demirtas

Abdullah Demirtas, Md, Assoc. Prof.

TC Erciyes University

研究点 (1)

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