Does End-fire Technique Increase Detection Rate of Prostate Cancer at First Re-biopsy Compared to Side-fire Technique?

Overview

Prostate cancer is the most common cancer among men in Sweden. During investigation of suspected cancer transrectal ultrasound with needle biopsies from prostate leeds to diagnosis. The most common technique today is side-fire where the needle enter the prostate in angle from the probe. In end-fire technique the needle enters the prostate at tip of probe without angle. The difference in techniques side-fire vs. end-fire affects the possibility to reach the ventral and apical aspects of prostate. Today´s standard is at least five cores from each side of the prostate at first biopsy. If first sample is negative there will usually be another urological exam and a first re-biopsy. The study aim to compare these two methods in cancer detection. The investigators' hypothesis is that when using end-fire technique at first re-biopsy, investigators find more cancers compared to side-fire. Patients are prospectively randomized into two groups, both assessing 12 core biopsies according to study protocol. Primary endpoint is cancer detection. Data will be collected about patient age, PSA-level, prostate size, digital rectal exam, hypoechogenic zones and length of cancers.

Full Title of Study: “Does End-fire Technique Increase Detection Rate of Prostate Cancer at First Re-biopsy Compared to Side-fire Technique, in Investigating a Raised Prostatic Specific Antigen (PSA)?”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: March 2018

Arms, Groups and Cohorts

  • Side-fire
    • Using side-fire technique during transrectal ultrasound.
  • End-fire
    • Using end-fire technique during transrectal ultrasound.

Clinical Trial Outcome Measures

Primary Measures

  • Cancer detection
    • Time Frame: Study inclusion continues until 400 patients is included. Estimated time frame from study start 5 years.
    • After finished study inclusion, data will be analyzed and presented within 12-18 months.

Participating in This Clinical Trial

Inclusion Criteria

  • first re-biopsy – PSA over 3ng/ml – T1c to T2a palpatory finding Exclusion Criteria:

  • prostate cancer – T2b or more advanced cancer – more than one previous biopsy done

Gender Eligibility: Male

Minimum Age: N/A

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Kronoberg County Council
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Joakim Ortegren, Principal Investigator, Section of Urology, Department of Surgery, Växjö County Hospital, Växjö, Sweden

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