FlowOx-MS: Pilot Investigation to Evaluate FlowOx2.0™ for Experimental Treatment of Spasticity

Sponsor

Otivio AS (Industry)

Overall Status

Recruiting

CT.gov ID

NCT04904016

Collaborator

Haukeland University Hospital (Other)

Enrollment

Location

Arm

6.1

Anticipated Duration (Months)

1.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a descriptive, prospective, non-controlled clinical investigation to be conducted on approximately 10 enrolled subjects at one site at Haukeland University Hospital in Bergen, Norway. The target subjects are male or female, 18-70 years, diagnosed with MS according to revised McDonald criteria (9) with spasticity and pain associated with the spasticity. Spasticity is evaluated based on self-reported spasticity using the numerical rating scale (NRS) which describes the average score of spasticity over the last 24 hours at >4 (where the scale scores spasticity from 0-10, where 0 is no spasticity, and 10 is worst possible spasticity), - combined with pain in the lower extremities last 24 hours. The pilot investigation is done to evaluate if FlowOx2.0™ can be used to treat spasticity with concomitant pain in patients with multiple sclerosis, using intermittent negative pressure affecting arteriovenous reflex.

Condition or Disease	Intervention/Treatment	Phase
Multiple Sclerosis Spasticity, Muscle Pain	Device: FlowOx™	N/A

Study Design

Study Type:

Interventional

Anticipated Enrollment :

10 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Single Center, Open, Non-controlled Pilot Investigation to Evaluate FLowOx2.0™ for Experimental Treatment of Spasticity With Concomitant Pain in Multiple Sclerosis, Using Intermittent Negative Pressure Affecting Arteriovenous Reflex

Anticipated Study Start Date :

May 28, 2021

Anticipated Primary Completion Date :

Dec 1, 2021

Anticipated Study Completion Date :

Dec 1, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Intervention FlowOx treatment Each participating subject will be provided with one FlowOx™ system, which will be used about 1 hour per day every day of the week for a 4-week period with the option to extend the treatment time to up to 6 months if the patients would like to continue.	Device: FlowOx™ The FlowOx™ system generates a negative oscillating pressure which cause rapid fluctuations in blood flow in the leg and foot.

Arm

Intervention/Treatment

Experimental: Intervention FlowOx treatment

Each participating subject will be provided with one FlowOx™ system, which will be used about 1 hour per day every day of the week for a 4-week period with the option to extend the treatment time to up to 6 months if the patients would like to continue.

Device: FlowOx™

The FlowOx™ system generates a negative oscillating pressure which cause rapid fluctuations in blood flow in the leg and foot.

Outcome Measures

Primary Outcome Measures

Self-Reported Spasticity, using Numerical Rating Scale: [4 weeks]
The unabbreviated scale title: Numerical Rating Scale The minimum and maximum values: 0, 10 Higher scores mean a worse outcome. To evaluate change in self-reported spasticity using the numerical rating scale (NRS) over the last 24 hours after daily 1-hour self-treatment with FlowOx from baseline to week 4

Secondary Outcome Measures

Desire to continue treatment [4 weeks]
Proportion of patients who wish to continue treatment with FlowOx beyond 4 weeks
Self-Reported Spasticity, using Numerical Rating Scale [3 months, 6 months]
The unabbreviated scale title: Numerical Rating Scale The minimum and maximum values: 0, 10 Higher scores mean a worse outcome. To evaluate change in self-reported spasticity using the numerical rating scale (NRS) over the last 24 hours after daily 1-hour self-treatment with FlowOx compared to baseline
Spasticity - modified Ashworth Scale [4 weeks, 3 months and 6 months]
The unabbreviated scale title: Modified Ashworth Scale The minimum and maximum values: 0, 4 Higher scores mean a worse outcome. Change in spasticity measured by modified Ashworth scale from baseline to week 4, month 3 and month 6.
Self-reported pain using Numerical Rating Scale [4 weeks, 3 months and 6 months]
The unabbreviated scale title: Numerical Rating Scale The minimum and maximum values: 0, 10 Higher score means worse pain. To evaluate change in self-reported spasticity using the numerical rating scale (NRS) over the last 24 hours after daily 1-hour self-treatment with FlowOx from baseline.
T25-FW [4 weeks, 3 months, 6 months]
Change of Timed 25-Foot Walk (T25-FW) from baseline
Expanded Disability Status Scale [4 weeks, 3 months, 6 months]
The unabbreviated scale title: Expanded Disability Status Scale The minimum and maximum values: 0, 10 Higher score means worse disability status. Change of functional score measured by Expanded Disability Status Scale (EDSS) and compared to baseline
Self-reported sleep (NRS) [4 weeks, 3 months, 6 months]
The unabbreviated scale title: Numerical Rating Scale The minimum and maximum values: 0, 10 Higher score means worse sleep. Change in self reported sleep quality will measured by (NRS) and compared to baseline
Hospital Anxiety and Depression Scale [4 weeks, 3 months, 6 months]
The unabbreviated scale title: Hospital Anxiety and Depression Scale The minimum and maximum values: 0, 3 Higher score means worse outcome. The Scale has 14 questions, the scores will be summarized at each time point and compared to baseline
Fatigue Scale for Motor and Cognitive Functions [4 weeks, 3 months, 6 months]
The unabbreviated scale title: Fatigue Scale for Motor and Cognitive Functions (FSMC) The FSMC is an assessment of MS-related cognitive and motor fatigue. A Likert-type 5-point scale (ranging from 'does not apply at all' to 'applies completely') produces a score between 1 and 5 for each scored question. Thus minimum value is 20 (no fatigue at all) and maximum value is 100 (severest grade of fatigue). Two subscales (mental and physical fatigue) can be made. Items included in the subscale mental are 1-4-7-8-11-13-15-17-18-20 and items included in the subscale physical are 2-3-5-6-9-10-12-14-16-19. Changes in the scores will be compared to baseline.
Multiple Sclerosis Impact Scale (MSIS-29) [4 weeks, 3 months, 6 months]
The unabbreviated scale title: Multiple Sclerosis Impact Scale The minimum and maximum values: 1, 5 Higher score means worse condition. There are 29 questions, change in reported status will be compared to baseline
SDMT [4 weeks, 3 months, 6 months]
Change in cognition measured by the Symbol Digit Modalities Test (SDMT) The Symbol Digit Modalities Test (SDMT) is a cognitive task. It consists of a sheet of paper with, at the top, a sequence of nine symbols and nine corresponding numbers (key). The task sequence consists of a series of symbols, each with a blank space underneath. Within a 90-second time limit the subject is required, consulting the key as necessary, to insert the numbers associated with the symbols. Changes in the performance will be compared to baseline.
Change in medication [4 weeks, 3 months and 6 monhts]
Medication used by the patients at the start of the trial will be recorded. Any change in frequency of use or dose of the medication to treat spasticity an/or pain will be recorded and compared to baseline.
Compliance [4 weeks, 3 months, 6 months]
"Compliance" / use of FlowOx, is automatically logged in the machine and will be read after 4 weeks
Safety- Incidence of device related adverse and serious adverse events [4 weeks, 3 months, 6 months]
The number and type of adverse events and servere device related events during the study will be recorded. To evaluate safety of FlowOx by assessment of device deficiencies and adverse events, non-serious and serious, rated for causality

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 70 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Diagnose MS according to revised McDonald criteria
Give written informed consent.
Have an age between 18-70 years.
Have stable disease without attack or progression of loss of function in the last three months.
Have self-reported spasticity, scored using the numeric rating scale (NRS) which describes the average score of spasticity over the last 24 hours, at ≥ 4 (where the scale scores spasticity from 0-10, where 0 is no spasticity, and 10 is worst possible spasticity), - combined with pain in the lower extremities last 24 hours
Have tried standard treatment for spasticity and pain without achieving a satisfactory effect.
Stable and unchanged treatment of spasticity and pain the last month
Stable and unchanged disease-modulating treatment for MS last 6 months.
Function level measured by the Expanded Disability Status Scale (EDSS) 2.0-6.5
Can self-manage study equipment.

Exclusion Criteria:

Have spasticity due to a disease other than MS.
Pregnancy or plan a pregnancy within the upcoming study period of 6 months.
Have an ongoing infection.
Have received botulinum toxin injection for spasticity within the last 4 months.
Have symptoms or illness that make it difficult to participate in the study.
Having planned surgery or other treatment within the coming study period of 6 months makes it difficult to participate in the study.
Have functional scores outside inclusion criteria measured by EDSS 2.0-6.5
Have had disease activity beyond requirements for stable disease as described in inclusion criteria
Have changed drug treatment beyond requirements for stable treatment as described in inclusion criteria.