The Composite Steep-pulse Treatment Apparatus Used in Prostate Cancer Ablation Therapy
Primary Purpose
Prostate Cancer
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Steep Pulse Device
Sponsored by
About this trial
This is an interventional treatment trial for Prostate Cancer focused on measuring focal therapy, IRE, Composite Steep-pulse Treatment Apparatus, prostate cancer, Multi-center
Eligibility Criteria
Inclusion Criteria:
- The therapy must be thoroughtly understood with the agreement signed
- Prostate MRI can identify negative extracapsular extension and seminal vesicle involvement,and no evidence of lymphatic metastasis
- Patients must have confirmed prostate cancer by prostate maping biopsy
- Low-risk or intermediate risk prostate cancer(PSA<20ng/ml,T1a-T2c,Gleason Score≤7)
- There must be no evidence of metastatic disease as confirmed by ECT and whole-body MRI
- No prostatic calculus or prostatic calculus≤5mm
- Age ≥ 40 - ≤ 85 years
- Life expectancy of greater than 5 years(WHO Performance Status 0-1)
- Patients with fertility are willing to take contraceptive measures until the end of the trial
Exclusion Criteria:
- Patients have previously undergone radical prostatectomy, hormonal therapy or radiotherapy.
- Patients underwent other surgery before less than 3 months.
- Patients required long-term medication with anticoagulans or stop taking anticoagulans less than 1 months
- Patients with clinically significant cardiovascular disease or other serious diseases
- Patients with metal implants in their bodys(for example,cardiac pacemaker ) and/or with metal implants which located in the range from the first lumbar vertebra(L1) to the middle of femurs.
- Patients with history of epilepsy
- Patients with other malignant tumor or patients with hiv.
- Patients with other serious systemic diseases that the study believes may interfere with the treatment, evaluation, and compliance of the trial;
- Patients with participation in another clinical trial less than 3 months.
- Patients with the judge that they are not suitable for this clinical trial
Sites / Locations
- Changhai Hospital,Second Military Medical University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Steep Pulse Device
Arm Description
Applying the steep pulse to treat the patients with Prostate cancer
Outcomes
Primary Outcome Measures
The result of prostate maping biopsy
evaluation of pathological analysis from the biopsy sample to confirm if there remain clinically significant prostate cancer
The result of prostate MRI
evaluation of ablation range from prostate MRI to confirm if there remain suspicious lesions
Secondary Outcome Measures
urinary incontinence
The rate of urinary incontinence
urination function(IPSS scoring)
evaluation of urination function by IPSS scoring
sexual function (IIEF-5 scoring)
evaluation of sexual function by IIEF-5 scoring
urinary catheter retention time
Record of urinary catheter retention time
Full Information
NCT ID
NCT03838432
First Posted
October 18, 2018
Last Updated
December 14, 2019
Sponsor
Second Military Medical University
Collaborators
RenJi Hospital, Peking Union Medical College Hospital, Zhejiang University
1. Study Identification
Unique Protocol Identification Number
NCT03838432
Brief Title
The Composite Steep-pulse Treatment Apparatus Used in Prostate Cancer Ablation Therapy
Official Title
The Efficacy and Safety of Composite Steep-pulse(High-frequency Irreversible Electroporation) Treatment Apparatus Used in Prostate Cancer Ablation Therapy : a Multicenter, Single-arm, Objective Performance Criteria Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 2, 2018 (Actual)
Primary Completion Date
September 27, 2019 (Actual)
Study Completion Date
January 18, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Second Military Medical University
Collaborators
RenJi Hospital, Peking Union Medical College Hospital, Zhejiang University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This trial is studying the effects and safety in treating patients from five different centers with local prostate cancer, employing Composite Steep-pulse(High-frequency irreversible electroporation) Treatment Apparatus. This device could cause cell irreversible electroporation, which leading necrosis of tumor cells. It also has the ability to prevent nerve,vessel, urethral and capsule unnecessary injury beside the ablation area. Composite Steep-pulse Treatment Apparatus will be used in patients who pass inclusion/exclusion criteria. Safety, quality of life, and histopathological analysis of prostate speciem will be evaluated in each study patients.
Detailed Description
Background:
Prostate cancer is the most common cancer in elderly males in western country. It is also a major health concern, especially in China with its greater proportion of elderly men in the general population. Currently, radical prostatectomy(RP) is the mainstream treatment for localized PCa to show a benefit for cancer-specific survival (CSS). However, the patient who underwent RP might suffer from the complication of erectile dysfunction or urinary incontinence. In 2004, a new method using steep pulses to treat tumor was appeared. It showed that steep pulses could bring about Irreversible Electroporation (IRE) of cell, leading tonecrosis of tumor cells. And it seemed to do no harms to the nerve and Vascular epithelial cell. The device of steep pulse had already been approved by FDA in 2011.However, this device of steep pulse has disadvantages like: (1)sever muscle contraction;(2)Urethral injury; (3)Capsule injury;(4)Nerve degeneration. This new device which is called Composite Steep-pulse(High-frequency irreversible electroporation) Treatment Apparatus, may have the potential to conquer these disadvantages.
Purpose:
This study will assess the efficacy of Composite Steep-pulse(High-frequency irreversible electroporation) Treatment Apparatus in the treatment of PCa.
This study will assess the safety of Composite Steep-pulse(High-frequency irreversible electroporation) Treatment Apparatus in the treatment of PCa.
Methods:
patients recruitment
transperineal maping prostate biopsy(>20 needle) guided by transrectal ultrasound(TRUS).
Irreversible Electroporation of malignant Tumor Cell under Composite Steep-pulse Treatment for the patients with positive biopsy;
Some factors such as prostate MRI,the maping prostate biopsy(>20 needle),the histopathological outcomes analysis ect. will be performed to evaluate the efficacy of the treatment.
Other factors such as the routine blood test, the routine urine test, the urinary continence ect. will be performed to evaluate the safety of the treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
focal therapy, IRE, Composite Steep-pulse Treatment Apparatus, prostate cancer, Multi-center
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
119 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Steep Pulse Device
Arm Type
Experimental
Arm Description
Applying the steep pulse to treat the patients with Prostate cancer
Intervention Type
Device
Intervention Name(s)
Steep Pulse Device
Intervention Description
Applying the steep pulse to treat the patients with Prostate cancer
Primary Outcome Measure Information:
Title
The result of prostate maping biopsy
Description
evaluation of pathological analysis from the biopsy sample to confirm if there remain clinically significant prostate cancer
Time Frame
6 Months
Title
The result of prostate MRI
Description
evaluation of ablation range from prostate MRI to confirm if there remain suspicious lesions
Time Frame
6 Months
Secondary Outcome Measure Information:
Title
urinary incontinence
Description
The rate of urinary incontinence
Time Frame
6 Months
Title
urination function(IPSS scoring)
Description
evaluation of urination function by IPSS scoring
Time Frame
6 Months
Title
sexual function (IIEF-5 scoring)
Description
evaluation of sexual function by IIEF-5 scoring
Time Frame
6 Months
Title
urinary catheter retention time
Description
Record of urinary catheter retention time
Time Frame
6 Months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The therapy must be thoroughtly understood with the agreement signed
Prostate MRI can identify negative extracapsular extension and seminal vesicle involvement,and no evidence of lymphatic metastasis
Patients must have confirmed prostate cancer by prostate maping biopsy
Low-risk or intermediate risk prostate cancer(PSA<20ng/ml,T1a-T2c,Gleason Score≤7)
There must be no evidence of metastatic disease as confirmed by ECT and whole-body MRI
No prostatic calculus or prostatic calculus≤5mm
Age ≥ 40 - ≤ 85 years
Life expectancy of greater than 5 years(WHO Performance Status 0-1)
Patients with fertility are willing to take contraceptive measures until the end of the trial
Exclusion Criteria:
Patients have previously undergone radical prostatectomy, hormonal therapy or radiotherapy.
Patients underwent other surgery before less than 3 months.
Patients required long-term medication with anticoagulans or stop taking anticoagulans less than 1 months
Patients with clinically significant cardiovascular disease or other serious diseases
Patients with metal implants in their bodys(for example,cardiac pacemaker ) and/or with metal implants which located in the range from the first lumbar vertebra(L1) to the middle of femurs.
Patients with history of epilepsy
Patients with other malignant tumor or patients with hiv.
Patients with other serious systemic diseases that the study believes may interfere with the treatment, evaluation, and compliance of the trial;
Patients with participation in another clinical trial less than 3 months.
Patients with the judge that they are not suitable for this clinical trial
Facility Information:
Facility Name
Changhai Hospital,Second Military Medical University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200000
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
35793110
Citation
Wang H, Xue W, Yan W, Yin L, Dong B, He B, Yu Y, Shi W, Zhou Z, Lin H, Zhou Y, Wang Y, Shi Z, Ren S, Gao X, Wang L, Xu C. Extended Focal Ablation of Localized Prostate Cancer With High-Frequency Irreversible Electroporation: A Nonrandomized Controlled Trial. JAMA Surg. 2022 Aug 1;157(8):693-700. doi: 10.1001/jamasurg.2022.2230.
Results Reference
derived
PubMed Identifier
34858837
Citation
He BM, Xue W, Yan WG, Yin L, Dong BJ, Zhou ZE, Lin HZ, Zhou Y, Wang YQ, Shi ZK, Zhou H, Wang SD, Ren SC, Gao X, Wang LH, Xu CL, Wang HF. A Multicenter Single-Arm Objective Performance Criteria Trial to Determine the Efficacy and Safety of High-Frequency Irreversible Electroporation as Primary Treatment for Localized Prostate Cancer: A Study Protocol. Front Oncol. 2021 Nov 10;11:760003. doi: 10.3389/fonc.2021.760003. eCollection 2021.
Results Reference
derived
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The Composite Steep-pulse Treatment Apparatus Used in Prostate Cancer Ablation Therapy
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