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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 University2 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
2
主要终点
To detect painful steps of biopsy procedure by asking patients verbally

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

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

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

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)

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 (2)

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