Efficacy and Safety Assessment of IRE of Localized Prostate Cancer.
Primary Purpose
Prostate Cancer, Prostate Adenocarcinoma
Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Focal irreversible electroporation of the prostate cancer
Sponsored by

About this trial
This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate, Irreversible Electroporation, Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Verified with MR-fusion biopsy localized Pca
- PSA < 15 ng/ml
- Gleason score 3+3=6; 3+4=7 OR Grade Group 1 and 2
- Life expectancy > 10 years
- No post-void residual urine or infravesical obstruction
Exclusion Criteria:
- patients with artificial cardiac pacemaker
- patients without rectum
- patients not eligible for general anesthesia
- PIRADS<3
- patients after primary Pca treatment
- hormonal therapy six months before the study
- radiotherapy of pelvic organs
- urinary infection
- extracapsular Pca
- patients with metastatic lesions
Sites / Locations
- Clinic of Urology, Sechenov University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
IRE patients
Arm Description
patients who will underwent 'Focal irreversible electroporation of the prostate cancer'
Outcomes
Primary Outcome Measures
PSA level
Stable decrese of PSA level after surgery (<1 ng/ml)
Complications
Short and long term surgical complications
Secondary Outcome Measures
IPSS (International Prostate Symptom Score, range from 5 to 30)
International Prostate Symptom Score
QoL (Quality of Life score, range 1-6)
Quality of Life Score
Qmax
Maximal urine flow rate
IIEF
International Index of Erectile Function - Erectile function assessment (range 1-5)
Full Information
NCT ID
NCT03504995
First Posted
April 12, 2018
Last Updated
July 27, 2020
Sponsor
I.M. Sechenov First Moscow State Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03504995
Brief Title
Efficacy and Safety Assessment of IRE of Localized Prostate Cancer.
Official Title
Efficacy and Safety Assessment of Nanoknife (AngyoDynamics, USA) for Irreversible Electroporation (IRE) of Localized Prostate Cancer.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 19, 2018 (Actual)
Primary Completion Date
April 30, 2020 (Actual)
Study Completion Date
April 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
I.M. Sechenov First Moscow State Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate safety and short-term oncological efficacy of the NanoKnife Irreversible Electroporation System for localised prostate cancer.
Irreversible electroporation (IRE) is the method of focal treatment for prostate cancer, which is already proven by FDA as method of the surgical ablation of soft tissue. It has not received clearance for the therapy or treatment of any specific disease or condition.
Detailed Description
Irreversible electroporation is a newly developed non-thermal tissue ablation technique in which short duration electrical fields are used to form permanent nanoscale defects in the cell membrane which leads to cell apoptosis. Thus, IRE is a non-thermal technique, which means that changes associated with tissue freezing or heating are not relevant.
Moreover, animal studies of IRE in the canine prostate have demonstrated that structures such as ejaculatory ducts, neurovascular bundles, blood vessels, and the urethra heal normally after ablation. The reason is that collagen matrix during treatment with IRE is not destroyed thus allowing for a large structures (blood vessels, nerves, etc.) to heal normally.
This study is a prospective and non-randomized with one group of 10 patients eligible for focal therapy of prostate cancer with IRE (eligibility defined by this protocol).
Before the surgery all patients will underwent transperineal MRI-fusion biopsy to localize the prostate cancer foci.
Objectives of the study: to asses safety of IRE in patients with localized PCa, to asses short-term oncologic efficacy of IRE in patients with localized PCa, to asses functional outcomes after IRE.
All patients will be followed up for 1 year (each 3 months).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Prostate Adenocarcinoma
Keywords
Prostate, Irreversible Electroporation, Prostate Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
IRE patients
Arm Type
Experimental
Arm Description
patients who will underwent 'Focal irreversible electroporation of the prostate cancer'
Intervention Type
Device
Intervention Name(s)
Focal irreversible electroporation of the prostate cancer
Intervention Description
Irreversible electroporation is a non-thermal tissue ablation technique in which short duration electrical fields are used to permanently permeabilize the cell membrane.
Primary Outcome Measure Information:
Title
PSA level
Description
Stable decrese of PSA level after surgery (<1 ng/ml)
Time Frame
3 months, 6 months, 9 months, 12 months.
Title
Complications
Description
Short and long term surgical complications
Time Frame
1 year
Secondary Outcome Measure Information:
Title
IPSS (International Prostate Symptom Score, range from 5 to 30)
Description
International Prostate Symptom Score
Time Frame
1 year
Title
QoL (Quality of Life score, range 1-6)
Description
Quality of Life Score
Time Frame
1 year
Title
Qmax
Description
Maximal urine flow rate
Time Frame
1 year
Title
IIEF
Description
International Index of Erectile Function - Erectile function assessment (range 1-5)
Time Frame
1 year
10. Eligibility
Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Verified with MR-fusion biopsy localized Pca
PSA < 15 ng/ml
Gleason score 3+3=6; 3+4=7 OR Grade Group 1 and 2
Life expectancy > 10 years
No post-void residual urine or infravesical obstruction
Exclusion Criteria:
patients with artificial cardiac pacemaker
patients without rectum
patients not eligible for general anesthesia
PIRADS<3
patients after primary Pca treatment
hormonal therapy six months before the study
radiotherapy of pelvic organs
urinary infection
extracapsular Pca
patients with metastatic lesions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dmitry Enikeev, MD, PhD
Organizational Affiliation
I.M. Sechenov First Moscow State Medcal University
Official's Role
Study Director
Facility Information:
Facility Name
Clinic of Urology, Sechenov University
City
Moscow
ZIP/Postal Code
119991
Country
Russian Federation
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
17668932
Citation
Rubinsky B. Irreversible electroporation in medicine. Technol Cancer Res Treat. 2007 Aug;6(4):255-60. doi: 10.1177/153303460700600401.
Results Reference
background
PubMed Identifier
29594551
Citation
Scheltema MJ, Chang JI, Bohm M, van den Bos W, Blazevski A, Gielchinsky I, Kalsbeek AMF, van Leeuwen PJ, Nguyen TV, de Reijke TM, Siriwardana AR, Thompson JE, de la Rosette JJ, Stricker PD. Pair-matched patient-reported quality of life and early oncological control following focal irreversible electroporation versus robot-assisted radical prostatectomy. World J Urol. 2018 Sep;36(9):1383-1389. doi: 10.1007/s00345-018-2281-z. Epub 2018 Mar 28.
Results Reference
background
Learn more about this trial
Efficacy and Safety Assessment of IRE of Localized Prostate Cancer.
We'll reach out to this number within 24 hrs