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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT05884580




Registration number
NCT05884580
Ethics application status
Date submitted
23/05/2023
Date registered
1/06/2023
Date last updated
24/11/2023

Titles & IDs
Public title
Neuflo System for the Treatment of BPH
Scientific title
Neuflo Water Electrolysis System for the Treatment of Benign Prostatic Hyperplasia
Secondary ID [1] 0 0
Neuflo-CIP-ANZ-202303
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Benign Prostatic Hyperplasia 0 0
Lower Urinary Tract Symptoms 0 0
Condition category
Condition code
Renal and Urogenital 0 0 0 0
Other renal and urogenital disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - Neuflo BPH Treatment System

Experimental: Participants receiving treatment with the Neuflo BPH Treatment System. -


Treatment: Devices: Neuflo BPH Treatment System
The Neuflo BPH Treatment System is designed to treat patients with lower urinary tract symptoms (LUTS) associated with BPH. It is an outpatient-based, minimally invasive treatment option and uses hydrolysis to reduce prostatic tissue in the lateral lobes of the prostate. Reduced pressure and constriction of the urethra alleviates urinary and other symptoms of BPH.
Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Effectiveness: Relief of BPH symptoms as measured by International Prostate Symptom Score (IPSS)
Timepoint [1] 0 0
3 months after treatment
Secondary outcome [1] 0 0
Improvement in urinary function (Qmax)
Timepoint [1] 0 0
At 3 months after treatment
Secondary outcome [2] 0 0
Improvement in urinary function (PVR)
Timepoint [2] 0 0
At 3 months after treatment
Secondary outcome [3] 0 0
Improvement in sexual function
Timepoint [3] 0 0
At 3 months after treatment
Secondary outcome [4] 0 0
Improvement in quality of life
Timepoint [4] 0 0
At 3 months after treatment
Secondary outcome [5] 0 0
Treatment tolerability & procedural medication requirements
Timepoint [5] 0 0
On day of treatment only
Secondary outcome [6] 0 0
Secondary intervention and medication use for Lower Urinary Tract Symptoms (LUTS)
Timepoint [6] 0 0
At 3, 6 and12 months after treatment
Secondary outcome [7] 0 0
Neuflo System performance
Timepoint [7] 0 0
On day of treatment only
Secondary outcome [8] 0 0
Neuflo System performance on Larger Prostates
Timepoint [8] 0 0
At 3 months after treatment
Secondary outcome [9] 0 0
Maintenance of improvement of LUTS
Timepoint [9] 0 0
At 12 months after treatment
Secondary outcome [10] 0 0
Participant satisfaction
Timepoint [10] 0 0
1 and 6 weeks, and 3, 6 and 12 months after treatment

Eligibility
Key inclusion criteria
Participants must meet all inclusion criteria to participate in this study.

1. Males aged 45 years of age or older

2. IPSS score of 13 or higher

3. Eligible uroflow with unadjusted or adjusted peak flow rate of equal to or less than
13ml/sec with a corresponding:

1. voided volume of at least 100 ml, and,

2. Post Void Residual (PVR) of 250 ml or less

4. Prostate volume of 25-80 cm3, inclusive as measured by ultrasound or MRI

5. Prostatic sagittal length of 3.2 cm or greater, as measured by ultrasound or MRI

6. Prostatic transverse width of 3.5 cm or greater as measured by ultrasound or MRI

7. Prostatic anterior-posterior height of 2.5 cm or greater as measured by ultrasound or
MRI

8. Participant must have the ability to understand and consent to participate in this
study

9. Participant must be willing and able to participate in follow-up evaluations
Minimum age
45 Years
Maximum age
No limit
Sex
Males
Can healthy volunteers participate?
No
Key exclusion criteria
Participants meeting any of the exclusion criteria listed at baseline will be excluded from
participation.

1. Outlet obstruction due to an enlarged middle lobe or significant central gland of the
prostate

2. Significant transverse asymmetry of prostatic lateral lobes

3. Participant has an implantable pacemaker or cardiac defibrillator

4. Participant has a penile implant

5. History or current diagnosis of prostate cancer or bladder cancer

6. Active urinary tract infection (UTI) (Note: participant can be enrolled if the UTI is
treated and followed with a negative urine test result)

7. Neurogenic, decompensated, or atonic bladder

8. Overactive bladder in the absence of prostatic obstruction

9. Current, recurrent (two or more) urethral strictures or muscle spasms that prevent
insertion of the catheter

10. Bleeding disorders or takes anticoagulation medications unless anti-platelet
medication has been discontinued for at least 7 days prior to treatment (Participants
are allowed to delay or repeat screening to fulfil this requirement)

11. Previous rectal surgery other than haemorrhoidectomy

12. Previous radical pelvic surgery or pelvic irradiation

13. Interest in maintaining fertility

14. Previous surgery or minimally invasive procedure(s) to treat symptomatic BPH

15. Use of Alpha blocker for the treatment of BPH within 14 days of treatment date.
(Participants are allowed to delay or repeat screening to fulfil this requirement)

16. 5-ARI (5-alpha-reductase inhibitor), (an enzyme inhibitor) use within 3 months of
treatment date (Participants are allowed to delay screening to fulfil this
requirement)

17. Concomitant bladder stones

18. History of other diseases or conditions causing voiding dysfunction

19. Current medication affecting bladder function

20. Known allergy to nickel

21. Chronic prostatitis, recurrent prostatitis, chronic pelvic pain syndrome (CPPS), or
painful bladder syndrome within the past 12 months

22. History of medical, surgical, or other conditions that, in the opinion of the
investigator, would limit study participation

Study design
Purpose of the study
Treatment
Allocation to intervention
N/A
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
1/12/2023
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/12/2024
Actual
Sample size
Target
25
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
New Zealand
State/province [1] 0 0
Tauranga

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
ProstaCare Pty Ltd
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The goal of this clinical study is to assess the effectiveness and safety of the Neuflo
System for the treatment of benign prostatic hyperplasia (BPH). The main questions it aims to
answer are:

- Can treatment with the Neuflo System lead to at least a 30% improvement in lower urinary
tract symptoms (LUTS) secondary to BPH, as measured by the international prostate
symptom score (IPSS) at 3 months after treatment which is sustained for 12 months?

- Is treatment with the Neuflo System tolerable to the patient, as measured by visual
analog score (VAS) for pain before and after treatment and procedural medication
requirements?

- Is treatment with the Neuflo System safe, as measured by the incidence and severity of
device or procedural related serious adverse events.

Participants will be enrolled in the study over a 6 month period. Each participant will be
treated with the Neuflo System and assessed at 3 and 12 months following treatment. A
subgroup of patients will have an MRI at 1 week to assess the volume and location of ablated
tissue.

The duration of the study is expected to be 18 months.
Trial website
https://clinicaltrials.gov/ct2/show/NCT05884580
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Flora Yuen
Address 0 0
Country 0 0
Phone 0 0
+61 2 9460 6688
Fax 0 0
Email 0 0
flora.yeun@avaniaclinical.com
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT05884580