New Biopsy Needle - Evaluation of Prostate Biopsy Quality
Primary Purpose
Prostate Cancer (Diagnosis)
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
TRUSbx
Sponsored by
About this trial
This is an interventional other trial for Prostate Cancer (Diagnosis) focused on measuring biopsy quality
Eligibility Criteria
Inclusion Criteria:
- Eligible for prostate biopsy
- Signed informed written consent
Exclusion Criteria:
- None (other than general contra indications for prostate biopsy or patient not willing to participate)
Sites / Locations
- Helsingborg Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
novel needle
standard tru cut needle
Arm Description
TRUSbx using the 18 gauge (G) 25 centimeter(cm) novel needle with 19 millimeter (mm) sample notch and a new actuator. 12 biopsies / patient.
TRUSbx using a standard tru cut biopsy needle (Mermaid Medical M-biopsy 18G 25 cm biopsy needle with a 19 mm sample notch) in a standard actuator ( Moller Medical Blue RBG-1000-10-1000). 12 biopsies/ patient.
Outcomes
Primary Outcome Measures
prostate biopsy length (measured by pathologist)
Length of biopsy specimen in millimeters
Secondary Outcome Measures
prostate biopsy fragmentation
The number of sections the biopsy specimen is made of
General appearance of biopsy assessed by pathologist (biopsy quality)
General quality of biopsy specimen on a scale from 0-3 (no biopsy, poor, good, excellent)
prostate biopsy length (measured in biopsy needle chamber)
Length of biopsy specimen in millimeters
prostate biopsy length (measured in after removal from biopsy chamber)
Length of biopsy specimen in millimeters
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04091230
Brief Title
New Biopsy Needle - Evaluation of Prostate Biopsy Quality
Official Title
Prospective Patient Blinded Randomized Trial Comparing Biopsy Specimen Quality in a Novel Biopsy Needle and Actuator Compared to Todays Standard Tru Cut Needle and Actuator.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
September 10, 2019 (Actual)
Primary Completion Date
October 30, 2019 (Actual)
Study Completion Date
November 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patient blinded randomized prospective trial evaluating prostate biopsy quality of a novel biopsy needle.
Detailed Description
Prostate biopsy is the golden standard for diagnose of prostate cancer. Transrectal prostate biopsy (TRUSbx) is the most widely used technique. Due to the transrectal path the biopsy needle will bring bacteria from the colon into tissue. The patent should always receive prophylactic antibiotics to reduce the risk of clinical infection. Infections related to transrectal prostate biopsy (TRUSbx) are increasing in parallel with rising antibiotic resistance.
The investigators have in an ex-vivo setting previously shown a drastic reduction in bacterial transfer across the colon wall using a novel biopsy needle designed to minimize bacterial transfer. Biopsy of prostatectomy specimen using the novel needle has shown biopsy quality equal to the tru cut biopsy needle used today.
This is the first human pilot aiming to evaluate if biopsy quality of the novel needle is equal to the reference tru cut biopsy needle in prostate biopsy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer (Diagnosis)
Keywords
biopsy quality
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
20 patients eligible for prostate biopsy are randomized into 2 arms (10+10 patients) using either the novel needle and actuator device or standard tru cut needle and actuator device used in the clinic today. On average 12 biopsies are taken from each patient. Biopsy quality is evaluated by the pathologist blinded to device used.
Masking
ParticipantOutcomes Assessor
Masking Description
Patient and pathologist are unaware of which needle/device is used. TRUSbx are taken from behind the back of the patient enabling masking from the patient.
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
novel needle
Arm Type
Experimental
Arm Description
TRUSbx using the 18 gauge (G) 25 centimeter(cm) novel needle with 19 millimeter (mm) sample notch and a new actuator. 12 biopsies / patient.
Arm Title
standard tru cut needle
Arm Type
Active Comparator
Arm Description
TRUSbx using a standard tru cut biopsy needle (Mermaid Medical M-biopsy 18G 25 cm biopsy needle with a 19 mm sample notch) in a standard actuator ( Moller Medical Blue RBG-1000-10-1000). 12 biopsies/ patient.
Intervention Type
Device
Intervention Name(s)
TRUSbx
Other Intervention Name(s)
prostate biopsy
Intervention Description
Trans Rectal UltraSound guided Prostate Biopsy
Primary Outcome Measure Information:
Title
prostate biopsy length (measured by pathologist)
Description
Length of biopsy specimen in millimeters
Time Frame
within 21 days post biopsy
Secondary Outcome Measure Information:
Title
prostate biopsy fragmentation
Description
The number of sections the biopsy specimen is made of
Time Frame
within 21 days post biopsy
Title
General appearance of biopsy assessed by pathologist (biopsy quality)
Description
General quality of biopsy specimen on a scale from 0-3 (no biopsy, poor, good, excellent)
Time Frame
within 21 days post biopsy
Title
prostate biopsy length (measured in biopsy needle chamber)
Description
Length of biopsy specimen in millimeters
Time Frame
within 21 days post biopsy
Title
prostate biopsy length (measured in after removal from biopsy chamber)
Description
Length of biopsy specimen in millimeters
Time Frame
within 21 days post biopsy
Other Pre-specified Outcome Measures:
Title
patient experience / pain
Description
Numeric rating Pain Scale rating from 0-10
Time Frame
at the time of rectal ultrasound probe insertion, estimated to a timeframe of 5-30 seconds.
Title
patient experience / pain
Description
Numeric rating Pain Scale rating from 0-10
Time Frame
at the time of injection needle advancement and periprostatic injection of local anesthesia, estimated to a timeframe of 5-10 seconds
Title
patient experience / pain
Description
Numeric rating Pain Scale rating from 0-10
Time Frame
at the time of biopsy sampling.
Title
14 day complications
Description
Any complications related to the biopsy (example infection, bleeding)
Time Frame
14 days
Title
30 day complications
Description
Any complications related to the biopsy (example infection, bleeding)
Time Frame
30 days
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Prostate Biopsy
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Eligible for prostate biopsy
Signed informed written consent
Exclusion Criteria:
None (other than general contra indications for prostate biopsy or patient not willing to participate)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam Linder, MD, PhD
Organizational Affiliation
Lund University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helsingborg Hospital
City
Helsingborg
State/Province
Scania
ZIP/Postal Code
254 37
Country
Sweden
12. IPD Sharing Statement
Plan to Share IPD
No
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New Biopsy Needle - Evaluation of Prostate Biopsy Quality
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