ClariCore System Used in Transperineal Prostate Biopsy

NCT ID: NCT03734575

Last Updated: 2019-07-11

Basic Information

• Recruitment Status: SUSPENDED
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-10-10
• Study Completion Date: 2019-07-09

Brief Summary

The overall objective of this study is to acquire ultrasound images, spectral data and prostate tissue biopsy cores using the ClariCore System via a transperineal approach.

Detailed Description

The overall objective of this study is to acquire ultrasound images, spectral data and prostate tissue biopsy cores using the ClariCore System via a transperineal approach. Ultrasound images corresponding to each needle insertion and T2-weighted MR scans will be saved for the purpose of further algorithm development that will provide physicians with real time tissue classification in conjunction with location information from the ultrasound imaging.

Conditions

Prostate Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

ClariCore System

Biopsy tissue, correlative spectral data, T2-weighted MR scans and ultrasound images acquired with the ClariCore System will be collected and recorded during standard practice transperineal biopsy.

Group Type: EXPERIMENTAL

ClariCore System

Intervention Type: DEVICE

The user will perform a standard trans-perineal biopsy and collect a number of biopsy cores as per standard practice.

Interventions

ClariCore System

The user will perform a standard trans-perineal biopsy and collect a number of biopsy cores as per standard practice.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Males per Investigator assessment appropriate for transperineal prostate biopsy

2. Patient scheduled for transperineal prostate biopsy based on standard of care urologic requirements to assess for tissue malignancy

3. Prostate volume > 20cc and length at least 22mm as verified by ultrasound or prostate MRI prior to the procedure

4. Patient must be able to provide legal consent and signs an IRB (Institutional Review Board)/EC (Ethics Committee) approved Informed Consent form to participate in the study prior to any study mandated determinations or procedure

Exclusion Criteria

1. Any anatomical or co-morbidity contraindications to transperineal prostate biopsy or transperineal prostate mapping biopsy

2. Acute painful perianal disorder (i.e. rectal abscess)

3. Symptomatic, acute prostatitis

4. Surgical absence of a rectum or the presence of a rectal fistula

5. Patient has systemic infection or evidence of any surgical site infection (superficial or organ space), including active urinary tract infection

6. Previous prostate intervention [TURP (bipolar, monopolar, laser)] TUMT, HIFU, Cryo, Rezum, Urolift], not including previous prostate biopsy

7. Current required use of blood thinning agents for medical comorbidity which prohibits the cessation of use as typically required per standard of care (SOC) prior to a medical procedure; or history of a bleeding disorder (e.g. coagulopathy)

8. Prior pelvic irradiation

9. Actively receiving therapy for the treatment of cancer (except for patients on 5-alpha reductase inhibitors, or non-melanoma skin cancers that are managed nonsystemically)

10. Actively receiving intravesical therapy or within 6 months of treatment for bladder cancer

11. Patient has compromised immune system, in the opinion of the Investigator

12. Active inflammatory bowel disease within the last 6 months

13. Any condition, or history of illness or surgery that, in the opinion of the Investigator, might confound the results of the study or pose additional risks to the patient (e.g.

significant cardiovascular conditions or allergies)

14. Patient is not likely to comply with the protocol or follow up evaluation

15. Patient is participating in a clinical trial of another investigational drug or device that may impact participation in this clinical study

• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Precision Biopsy, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

James Wysock, MD

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Urology Associates

Locations

The James Buchanan Brady Urological Institute and Department of Urology

Baltimore, Maryland, United States

NYU Langone Urology Associates

New York, New York, United States

Countries

United States

Other Identifiers

CIP-1012

Identifier Type: -

Identifier Source: org_study_id