Neurotech Vital Compact Versus Itouch Sure Pelvic Floor Exerciser US

Stress Urinary Incontinence Clinical Trial

Official title:

A Single-blind, Multi-centre, Randomised, Controlled, Non-inferiority, Clinical Study to Assess the Safety and Performance of the Neurotech Vital Compact Device Compared to the Itouch Sure Pelvic Floor Exerciser for the Treatment of Stress Urinary Incontinence in Female Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02423005
• Other study ID #: BMR-13-1001
• Status: Completed
• Phase: N/A
• First received: April 17, 2015
• Last updated: February 1, 2018
• Start date: April 2015
• Est. completion date: April 2017

Study information

• Verified date: February 2018
• Source: Atlantic Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A prospective, randomised, controlled, single-blind, multi-site clinical study employing Neuromuscular Electrical Stimulation (NMES) to stimulate the pelvic floor muscles of women suffering from stress urinary incontinence.

Approximately one-hundred and eighty (180) female patients diagnosed with stress urinary incontinence will be enrolled in this study. All patients who are considered eligible to participate in the clinical study and give consent will be randomised to complete either a 12-week treatment programme with the Neurotech Vital Compact device or a 12-week treatment programme with the itouch Sure Pelvic Floor Exerciser. The 12-week treatment programme will be completed by the subjects at home with treatment with the device in accordance with the device Instructions for Use.

Description:

This is a prospective, randomised, controlled, single-blind, multi-site clinical study to be conducted in the United States of America (USA) employing Neuromuscular Electrical Stimulation (NMES) to stimulate the pelvic floor muscles of women suffering from stress urinary incontinence.

Approximately one-hundred and eighty (180) female patients diagnosed with stress urinary incontinence will be enrolled in this study. All patients who are considered eligible to participate in the clinical study and give consent will be randomised to complete either a 12-week treatment programme with the Neurotech Vital Compact device or a 12-week treatment programme with the itouch Sure Pelvic Floor Exerciser. The 12-week treatment programme will be completed by the subjects at home with treatment with the device in accordance with the device Instructions for Use.

Subjects included in the clinical study will be evaluated at screening, on enrolment into the study (baseline) and during the 12-week treatment programme at 4 and 12 weeks. A telephone call will be made at 1 week to check on the patient's progress. In addition, subjects will be evaluated at 26 week following their commencement of the treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 180
• Est. completion date: April 2017
• Est. primary completion date: April 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Subjects who are female and at least 18 years of age, and not more than 65 years of age.

2. Subjects who have signed the informed consent form prior to any study related activity.

3. Subjects who have previously tried and failed to improve their condition using Kegel exercises.

4. Subjects who have been clinically diagnosed with stress urinary incontinence and demonstrate a greater than or equal to 3g urine leakage and a less than or equal to 90g urine leakage (>3g and < 90g) following a bladder-filling protocol and then a standardised stress test (provocative pad weight test) at the baseline assessment.

5. Subjects who score 9 or less (<9) out of 18 for the Urge Incontinence Questions and are confirmed as having predominant stress urinary incontinence on the Medical, Epidemiologic and Social Aspects of Aging Urinary Incontinence (MESA) Questionnaire completed at the screening assessment.

6. Subjects with a Body Mass Index of = 35 kg/m2.

7. Subjects of child-bearing potential who are using a highly effective contraceptive method (established use of oral, injected, implanted hormonal method of contraception or barrier method of contraception with spermicide).

8. Subjects who are willing not to seek any other treatment for stress incontinence during the study period.

9. Subjects who are able to give voluntary, written informed consent to participate in this study and from whom consent has been obtained.

10. Subjects who are able to understand this study and are willing to complete all the study assessments.

Exclusion Criteria:

1. Subjects who have an existing medical condition that would compromise their participation in the study, e.g. reduced sensory perception in the contact area of the stimulation electrodes; scars or vaginal tissue wounds, lesions or inflamed/infected areas in the contact area of the stimulation electrodes; vaginal bleeding between menstrual periods; uncontrolled diabetes.

2. Subjects who have a physical condition that would make them unable to perform the study procedures, e.g. pelvic or hip surgery within the past 6 weeks.

3. Subjects who have been diagnosed with Chronic Obstructive Pulmonary Disease (COPD).

4. Subjects with a history of an underlying neurological condition, e.g. Multiple Sclerosis, Parkinson's disease, epilepsy.

5. Subjects with any bladder abnormality that would affect the urinary flow through the lower urinary tract including signs or symptoms of an active urinary tract infection, abnormal bladder capacity (e.g., >300 cc), post void residual volume >200 cc, spastic bladder, vesico-ureteral reflux or bladder stones.

6. Subjects with a blood clotting disorder or who are taking anti-coagulant medications.

7. Subjects who have previously had any uro-gynaecological related surgery that would affect the pelvic floor muscles or urinary flow through the urethra (excluding hysterectomy).

8. Subjects who have previously had pelvic floor radiation.

9. Subjects who have previously been treated for stress incontinence with injectable bulking agents and/or vaginal probes within the past 6 months.

10. Subjects with a clinical diagnosis of prolapse greater than Stage 2.

11. Subjects who are pregnant or could be pregnant.

12. Subjects who are less than 6 months post-partum or who are lactating.

13. Subjects who have any conductive intra-uterine devices or metal implants in the pelvic area, including hip and lumbar spine.

14. Subjects with pelvic pain or fibromyalgia or paravaginal defect.

15. Subjects with an active implanted medical device (i.e. pacemaker, insulin pump etc.) or conditions that may be adversely affected by electrical stimulation (e.g. cardiac arrhythmias).

16. Subjects with a current or active history of pelvic cancer and/or subjects with a life expectancy of less than 12 months.

17. Subjects who are currently involved in any injury litigation claims.

18. Subjects who have participated in a clinical study in the last 3 months or any previous clinical study with Bio-Medical Research Ltd.

19. Subjects who have been committed to an institution by virtue of an order issued either by the courts or by an authority.

Related Conditions & MeSH terms

• Enuresis
• Stress Urinary Incontinence
• Urinary Incontinence
• Urinary Incontinence, Stress

Intervention

Device:
• Neurotech Vital Compact
Neuromuscular electrical stimulation of the pelvic floor via an arrangement of external electrodes held in place by a garment.
• itouch Sure Pelvic Floor Exerciser
Vaginal probe with electrodes designed to deliver electrical stimulation to the pelvic floor muscles.

Locations

Country	Name	City	State
United States	Boston Clinical Trials	Boston	Massachusetts
United States	Medical University of South Carolina	Charleston	South Carolina
United States	AccuMed Research Associates	Garden City	New York
United States	Hartford Hospital	Hartford	Connecticut
United States	The Jackson Clinic	Jackson	Tennessee
United States	Altus Research	Lake Worth	Florida
United States	University of California Irvine Medical Center	Orange	California
United States	Temple University	Philadelphia	Pennsylvania
United States	Maricopa Integrated Health Systems	Phoenix	Arizona
United States	Renaissance Health & Surgical Associates	South Pittsburg	Tennessee
United States	University of South Florida Medical Center	Tampa	Florida
United States	Lyndhurst Gynecological Associates	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Atlantic Therapeutics	Bio-Medical Research, Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of subjects who have achieved >50% improvement on the provocative pad weight test.	Subjects will complete an in-office 1 hour provocative pad test to determine volume of urine leaked during the test.	12 weeks
Secondary	Between group comparison of mean change in urine leakage in a provocative pad weight test	Comparison of change on 1 hour pad test for Vital Compact vs. itouch Sure	12 Weeks
Secondary	Within group comparison of mean change in urine leakage in the 1 hour pad weight test	Comparison of change in urine leakage for each treatment arm	12 weeks
Secondary	Between group comparison of the mean improvement in the Incontinence Quality of Life Questionnaire (I-QOL) score	Comparison of change in I-QOL score between groups	12 weeks
Secondary	Between group comparison of the proportion of subjects achieving dryness	The treatment arms will be compared regarding the proportion of subjects who leak less than 1 g at the 12 week 1 hour pad test.	12 weeks
Secondary	Between group comparison of mean change in the number of incontinence episodes per day.	Between group comparison of mean change in the number of incontinence episodes per day using a 7-day voiding diary.	12 weeks
Secondary	Between group mean change in urine leakage in the 24-hour pad weight test	Between group comparison of mean change, with respect to baseline, in urine leakage in the 24-hour pad weight test	12 weeks
Secondary	Within Neurotech Vital Compact group estimate of mean change in urine leakage in the 24-hour pad weight	• Within Neurotech Vital Compact group estimate of mean change, with respect to baseline, in urine leakage in the 24-hour pad weight	12 weeks
Secondary	Within Neurotech Vital Compact group estimate of mean improvement in Incontinence Quality of Life Questionnaire (I-QOL) score	Within Neurotech Vital Compact group estimate of mean improvement, with respect to baseline, in Incontinence Quality of Life Questionnaire (I-QOL) score	12 weeks
Secondary	Between group comparison of mean change in the number of pads used/day	Between group comparison of mean change, with respect to baseline, in the number of pads used/day recorded using a 7-day voiding diary	12 weeks
Secondary	Within Neurotech Vital Compact group estimate of mean change in the number of pads used/day	Within Neurotech Vital Compact group estimate of mean change, with respect to baseline, in the number of pads used/day recorded using a 7-day voiding diary	12 weeks
Secondary	Between group comparison of the proportion of subjects achieving dryness at Week 12 (<1g on the provocative pad weight test)	Between group comparison of the proportion of subjects achieving dryness at Week 12 (<1g on the provocative pad weight test)	12 weeks
Secondary	Comparison of adverse events	Comparison between groups of adverse events reported throughout the study.	6 months