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Efficacy and Safety Assessment of IRE of Localized Prostate Cancer.

Efficacy and Safety Assessment of Nanoknife (AngyoDynamics, USA) for Irreversible Electroporation (IRE) of Localized Prostate Cancer.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03504995
Enrollment
10
Registered
2018-04-20
Start date
2018-04-19
Completion date
2020-04-30
Last updated
2020-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Adenocarcinoma, Prostate Cancer

Keywords

Prostate, Irreversible Electroporation, Prostate Cancer

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).

Interventions

Irreversible electroporation is a non-thermal tissue ablation technique in which short duration electrical fields are used to permanently permeabilize the cell membrane.

Sponsors

I.M. Sechenov First Moscow State Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
PSA level3 months, 6 months, 9 months, 12 months.Stable decrese of PSA level after surgery (\<1 ng/ml)
Complications1 yearShort and long term surgical complications

Secondary

MeasureTime frameDescription
IPSS (International Prostate Symptom Score, range from 5 to 30)1 yearInternational Prostate Symptom Score
QoL (Quality of Life score, range 1-6)1 yearQuality of Life Score
Qmax1 yearMaximal urine flow rate
IIEF1 yearInternational Index of Erectile Function - Erectile function assessment (range 1-5)

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026