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Multicentric Comparative Prospective Study of the Benefits and Risks of Biopsy Prostate Using Transrectal or Transperineal Procedure for the Prostate Cancer Diagnostic (BIOPROSTABORD)

Primary Purpose

Patients With Suspected Prostate Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Biopsy
Sponsored by
Elsan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Patients With Suspected Prostate Cancer focused on measuring Transpérinéal, Transrectal, Biopsy, Prostate, Cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: Patients with suspected prostate cancer with at least one of the following criteria met : MRI Staging: T2 or T3a, MRI Grading: Pirads greater than or equal to 3 MRI tumor volume greater than or equal to 0.5 cm3 e.Patient without tumor lesion detected by prostate MRI less than 3 months old with PSA > 4 ng/ml, or an observed suspicious induration to the rectal exam Voluntarily signed and dated written informed consents prior to any study specific procedure, Exclusion Criteria: Other medical conditions may interfere with the conduct of the study and, in the judgment of the investigator, would make the patient inappropriate for entry into this study, Individuals deprived of liberty or placed under legal guardianship, Unwillingness or inability to comply with the study protocol for any reason. Patients without a health insurance

Sites / Locations

  • Clinique St Augustin
  • Centre Médico-Chirurgical Les Cèdres

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Transrectal biopsy using KOELIS fusion system

Transperineal biopsy using KOELIS perine grid

Arm Description

Transrectal procedure will be performed with the patient in the left lateral position with a completely free-hand technique utilising the KOELIS fusion system.

Transperineal biopsy will be performed in the lithotomy position. KOELIS "Perine Grid" needle guidance device and "Steady Pro" free-hand probe arm will be utilised (free-hand assisted technique).

Outcomes

Primary Outcome Measures

Comparison of the rate of occurrence of biopsy-induced infection in both groups
Biopsy-induced infection are defined as : Positive post-biopsy urinary test result Clinical infection syndrome (T>37.5°C fever) Signs of urogenital infection (cystitis/prostatitis/orchi-epididymitis) Hospitalization for hyperpyrexia Septic shock

Secondary Outcome Measures

Comparison of the rate of rectal bleeding in both groups
Comparison of the rate of urethral bleeding (hematuria and urethrorrhagia) in both groups
Comparison of the percentage of negative biopsies in both groups
Comparison of the percentage of positive biopsies on on anterior areas in both groups
Comparison of the Percentage of underestimation of the stage of tumor development in both groups
Confrontation with the MRI result and the resected specimen of the radical prostatectomy
Assess the pain (tolerance) felt by the patient according to the biopsy method used
EVA pain scale at J0
Comparison of the Room occupancy time in both groups
Comparison of the Procedure Time in both groups
Procedure time = Endorectal Ultrasound Probe Introduction Time - Probe Removal Time
Comparison of the Average Length of Stay in both groups

Full Information

First Posted
January 11, 2023
Last Updated
October 10, 2023
Sponsor
Elsan
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1. Study Identification

Unique Protocol Identification Number
NCT05763355
Brief Title
Multicentric Comparative Prospective Study of the Benefits and Risks of Biopsy Prostate Using Transrectal or Transperineal Procedure for the Prostate Cancer Diagnostic
Acronym
BIOPROSTABORD
Official Title
Multicentric Comparative Prospective Study of the Benefits and Risks of Biopsy Prostate Using Transrectal or Transperineal Procedure for the Prostate Cancer Diagnostic.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
September 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Elsan

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
The performance of prostatic biopsies is an essential element to confirm the diagnosis of prostate cancer and to specify the characteristics of the tumor in terms of stage and grade. The first route of prostatic biopsies is mainly transrectal with passage of a needle introduced into the guide fixed on the endorectal ultrasound probe. There is another possible access route, transperineal, with prostatic puncture by a needle introduced transcutaneously, guided by an endorectal ultrasound image. The first transperineal route would offer the first benefit for the patient, to reduce the infectious risk inherent in the endorectal way. It would also reduce the risk of rectal bleeding. In addition, the transperineal pathway appears to be able to improve the detection threshold of prostatic tumours located on the anterior part of the gland due to the angle of penetration of the needle and its more anterior positioning relative to the prostate. There is currently no randomized comparison study of the transperineal versus transrectal procedure on infectious risk. The aim of the project is to enable this comparative study, within our institution where experienced urologist surgeons practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients With Suspected Prostate Cancer
Keywords
Transpérinéal, Transrectal, Biopsy, Prostate, Cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
596 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Transrectal biopsy using KOELIS fusion system
Arm Type
Other
Arm Description
Transrectal procedure will be performed with the patient in the left lateral position with a completely free-hand technique utilising the KOELIS fusion system.
Arm Title
Transperineal biopsy using KOELIS perine grid
Arm Type
Other
Arm Description
Transperineal biopsy will be performed in the lithotomy position. KOELIS "Perine Grid" needle guidance device and "Steady Pro" free-hand probe arm will be utilised (free-hand assisted technique).
Intervention Type
Procedure
Intervention Name(s)
Biopsy
Intervention Description
Biopsies will be performed under local anaesthesia. In all patients with a suspicious lesion (PIRADSv2.1 3-5) noted on the mp-MRI, the software-based image fusion biopsies will be obtained collecting 3 to 5 cores per target area according to its volume, 10-12 systematic cores of the remaining areas of the prostate will be collected from sectors specified in the PIRADSv2.1 prostate map.
Primary Outcome Measure Information:
Title
Comparison of the rate of occurrence of biopsy-induced infection in both groups
Description
Biopsy-induced infection are defined as : Positive post-biopsy urinary test result Clinical infection syndrome (T>37.5°C fever) Signs of urogenital infection (cystitis/prostatitis/orchi-epididymitis) Hospitalization for hyperpyrexia Septic shock
Time Frame
30 days after intervention
Secondary Outcome Measure Information:
Title
Comparison of the rate of rectal bleeding in both groups
Time Frame
30 days after intervention
Title
Comparison of the rate of urethral bleeding (hematuria and urethrorrhagia) in both groups
Time Frame
30 days after intervention
Title
Comparison of the percentage of negative biopsies in both groups
Time Frame
30 days after intervention
Title
Comparison of the percentage of positive biopsies on on anterior areas in both groups
Time Frame
30 days after intervention
Title
Comparison of the Percentage of underestimation of the stage of tumor development in both groups
Description
Confrontation with the MRI result and the resected specimen of the radical prostatectomy
Time Frame
3 months after intervention
Title
Assess the pain (tolerance) felt by the patient according to the biopsy method used
Description
EVA pain scale at J0
Time Frame
1 day
Title
Comparison of the Room occupancy time in both groups
Time Frame
1 day
Title
Comparison of the Procedure Time in both groups
Description
Procedure time = Endorectal Ultrasound Probe Introduction Time - Probe Removal Time
Time Frame
1 day
Title
Comparison of the Average Length of Stay in both groups
Time Frame
1 day

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with suspected prostate cancer with at least one of the following criteria met : MRI Staging: T2 or T3a, MRI Grading: Pirads greater than or equal to 3 MRI tumor volume greater than or equal to 0.5 cm3 e.Patient without tumor lesion detected by prostate MRI less than 3 months old with PSA > 4 ng/ml, or an observed suspicious induration to the rectal exam Voluntarily signed and dated written informed consents prior to any study specific procedure, Exclusion Criteria: Other medical conditions may interfere with the conduct of the study and, in the judgment of the investigator, would make the patient inappropriate for entry into this study, Individuals deprived of liberty or placed under legal guardianship, Unwillingness or inability to comply with the study protocol for any reason. Patients without a health insurance
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre-Thierry PIECHAUD, MD
Phone
(0)6.09.71.58.67
Ext
+33
Email
pthpiechaud@hotmail.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Charlène PY, CRA
Phone
(0)7.64.51.03.73
Ext
+33
Email
charlene.py@elsan.care
Facility Information:
Facility Name
Clinique St Augustin
City
Bordeaux
ZIP/Postal Code
33074
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre-Thierry PIECHAUD, MD
Email
pthpiechaud@hotmail.fr
First Name & Middle Initial & Last Name & Degree
Pierre-Thierry PIECHAUD, MD
Facility Name
Centre Médico-Chirurgical Les Cèdres
City
Brive-la-Gaillarde
ZIP/Postal Code
19100
Country
France

12. IPD Sharing Statement

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Multicentric Comparative Prospective Study of the Benefits and Risks of Biopsy Prostate Using Transrectal or Transperineal Procedure for the Prostate Cancer Diagnostic

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