Performance and Long-term Safety of FlowOx2.0™ in Patients With Multiple Sclerosis - Impact on Spasticity and Pain (FO-NP002)

A Double-blind, Randomized, Controlled, Parallel Design 4-week Investigation, Followed by an Open 6-month Investigation, to Evaluate the Performance and Long-term Safety of FlowOx2.0™ in Patients With Multiple Sclerosis

The study is a 4-week double-blind, randomized, controlled, parallel design investigation to investigate the impact of intermittent negative pressure on spasticity and pain in people with multiple sclerosis (pwMS). The investigational device (FlowOx2.0™) is composed of a Pressure Chamber and a Control Unit (and disposable parts). All subjects will receive the same pressure chamber but be randomized to either a Control Unit that generates intermittent negative pressure (INP) of - (minus) 40 mmHg or a Control Unit that generates INP of - 10 mmHg. FlowOx2.0™ generating -40 mmHg is the investigational device, and FlowOx2.0™ generating -10 mmHg, is the comparator device. After the initial 4-week double-blind period, all participants will be offered the -40mmHg control unit to be used during a 6-months optional extension part.

Study Overview

• Status: Active, not recruiting
• Conditions: Multiple Sclerosis; Spasticity, Muscle; Pain, Chronic
• Intervention / Treatment: Device: FlowOx 2.0; Device: FlowOx2.0 (Sham)

Detailed Description

FlowOx2.0™ is a commercially available device for home treatment of peripheral arterial disease. It is designed to be used at home by patients and has been shown to cause rapid changes in blood flow velocity in the treated leg. Recently, individuals with multiple sclerosis have reported a positive impact on their self-perceived spasticity and pain levels. The purpose of this study is to control for potential placebo effects using a comparator device.

The study will recruit patients from Norway, Sweden, and Denmark. All subjects will be instructed to treat the most affected leg for 60 minutes per day, preferentially in the evening. The same leg should be treated throughout the study period. The 4-week double-blind part is immediately followed by an optional extension part. This part is an open investigation in which all randomized subjects that have completed the main part are offered to continue for an additional 6 months using the active device (INP pulses of - 40 mmHg).

• Study Type: Interventional
• Enrollment (Actual): 56
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Iacob Mathiesen, PhD; Phone Number: +47 46890416; Email: im@otivio.com
• Study Contact Backup: Name: Henrik Hoel, MD, PhD; Phone Number: +47 99305006; Email: hh@otivio.com

Study Locations

• Sweden
  • Stockholm, Sweden, 113 65
    • NeuroCentrum (Centrum för Neurologi)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

The subjects must meet all the following criteria to be eligible to participate in the clinical investigation:

1. Diagnosed MS according to revised McDonald criteria.
2. Give written informed consent.
3. Age 18-70 years.
4. Stable MS disease without attack within the last three months.

5. Ability to perform the walk tests:

   1. 2-minute walk test, and
   2. 25-Foot walk.
6. Self-reported spasticity in the most affected leg that would be subject to treatment at baseline with a score of ≥ 4, scored using the numeric rating scale (NRS) during the last 24 hours.
7. Pain and/or discomfort related to the spasticity described in inclusion criteria 6., over the last 7 days using the numeric rating scale (NRS).
8. Stable and unchanged treatment of spasticity and pain over the last month, as judged by the Investigator.
9. Stable and unchanged disease-modulating treatment for MS last 6 months, as judged by the Investigator.
10. Can self-manage study equipment.
11. Willingness and ability to comply with study procedures, visit schedules, and requirements.

Exclusion Criteria:

Subjects meeting any of the following criteria will not be permitted to participate in the clinical investigation:

1. Have spasticity due to a disease other than MS.
2. Pregnancy or planned pregnancy within the upcoming study period, up to 7 months (includes the optional extension part).
3. Have an ongoing infection that subjectively affects their MS state, as judged by the Investigator.
4. Have received botulinum toxin injection for spasticity within the last 4 months.
5. Have symptoms or illness that make it difficult to participate in the study, as judged by the Investigator.
6. Having planned surgery or other treatment within the coming study period of up to 7 months making it difficult to participate in the study, as judged by the Investigator.
7. Subjects with uncontrolled wound infections or infections in the skin of the treated leg.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Investigational device; The investigational device (FlowOx2.0) is composed of a Pressure Chamber and a Control Unit (and disposable parts). All subjects will receive the commercial Pressure Chamber (and disposable parts). Subjects randomized to the investigational device arm will receive a Control Unit that generates intermittent negative pressure (INP) of - (minus) 40 mmHg.	Device: FlowOx 2.0; Subjects randomized to tretament with the investigational device will receive treatment with -40 mmHg intermittent negative pressure for 60 minutes per day.; Other Names: Intermittent negative pressure (Active)
Sham Comparator: Comparator; The investigational device (FlowOx2.0) is composed of a Pressure Chamber and a Control Unit (and disposable parts). All subjects will receive the commercial Pressure Chamber (and disposable parts). Subjects randomized to the comparator arm will receive a Control Unit that generates INP pulses of only - (minus) 10 mmHg.	Device: FlowOx2.0 (Sham); Subjects randomized to treatment with the comparator will receive treatment with -10 mmHg intermittent negative pressure for 60 minutes per day.; Other Names: Intermittent negative pressure (Sham)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in self-reported spasticity using Numeric Rating Scale (NRS)	Numerical Rating Scale The minimum and maximum values: 0, 10 Higher scores mean a worse outcome the last 24 hours. The scale scores spasticity from 0-10, where 0 is no spasticity, and 10 is worst imaginable spasticity. The scoring should be done at roughly the same time of day and not during or immediately after treatment.	4 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in self-reported pain using NRS for subjects with a baseline NRS ≥4.	Pain is scored using the NRS which describes the average score of pain over the last 24 hours. The scale scores pain from 0-10, where 0 is no pain, and 10 is worst imaginable pain. The scoring is done each day of the study. The scoring should be done roughly at the same time and not during or immediately after treatment.	4 weeks
Frequency of adverse events	All incidences of adverse events (AEs) and device deficiencies (DDs) will be documented and reported during the clinical investigation. At visits and phone calls, study staff will ask whether the subject has experienced any AEs/DDs since the last call/visit. Staff will also follow-up any previous AEs during visits and calls, i.e., are AEs resolved or still ongoing. The subjects will also be encouraged to call and report between visits and calls.	4 weeks
Change in timed 25-foot walk (T25-FW)	The Timed 25-Foot Walk (T25-FW). The T25-FW is a quantitative mobility and leg function performance test based on a timed 25-Foot Walk. The subject is directed to one end of a clearly marked 25-foot course and is instructed to walk 25 feet as quickly as possible, but safely. The time is calculated from the initiation of the instruction to start and ends when the subject has reached the 25-foot mark. The task is immediately administered again by having the patient walk back the same distance. The "score" is the average of these two walks. Subjects may use assistive devices when doing this task. Staff record the average T25-FW score in seconds.	4 weeks
Change in 2-minute walking tests	The 2-min walk test, should be tested in a hallway free of obstacles. Subject instruction will be: "Cover as much ground as possible over 2 minutes. Walk continuously, if possible, but do not be concerned if you need to slow down or stop to rest. The goal is to feel at the end of the test that more ground could not have been covered in the 2 minutes."	4 weeks
Change in health-related quality of life measured by Multiple sclerosis impact scale (MSIS-29)	The MSIS-29 is a measure of the physical and psychological impact of multiple sclerosis (MS) from the patients' perspective. Twenty-nine (29) questions are responded by the subject by circling the number that best describes the subject's situation (graded 1-5, where 1 is "not at all" and 5 is extremely). It captures the subject's views about the impact of MS on his/her day-to-day life during the past two weeks.	4 weeks
Change in health-related quality of life measured by EQ-5D-5L	The EQ-5D-5L is a self-assessed, health related, quality of life questionnaire. The scale measures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The EQ-5D-5L essentially consists of 2 pages: the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS).	4 weeks
Change in Hospital Anxiety and Depression Scale (HADS)	The Hospital Anxiety and Depression Scale (HADS) is a 14-item measure designed to assess anxiety and depression symptoms in medical patients, with emphasis on reducing the impact of physical illness on the total score. Items are rated on a 4-point severity scale. The HADS produces two scales, one for anxiety (HADS-A) and one for depression (HADS-D), differentiating the two states.	4 weeks

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
The proportion of subjects with ≥ 30% improvement in self-reported pain using NRS	The endpoint will be assessed as described under the primary endpoint.	4 weeks
Mean daily treatment time	The control unit records daily use, frequency of use per day and errors (periods without predefined pressure generated). The data will be compiled and used to ensure compliance.	4 weeks
Proportion of subjects who wish to continue treatment with FlowOx2.0 beyond 4 weeks	The number of individuals interested in continuing treatment is expected to reflect a potential benefit. The information will be tabled.	4 weeks
Change in medication use for spasticity and pain	During the enrolment visit, medication use for spasticity and pain will be registered. The same will be recorded at subsequent visits.	4 weeks
Change of self-reported sleep quality using the NRS	Sleep quality is scored using the NRS which describes the average score of sleep over the last 24 hours. The scale scores sleep quality from 0-10, where 0 is the best possible sleep, and 10 is the worst imaginable sleep. The scoring should be done roughly at the same time during the day.	Beginning of every week for the first 4 weeks
Change in fatigue using the NRS	Fatigue is scored using the NRS which describes the average score of fatigue over the last 24 hours. The scale scores fatigue from 0-10, where 0 is no fatigue, and 10 is the worst imaginable fatigue. The scoring should be done roughly at the same time during the day.	Beginning of every week for the first 4 weeks
Subjects experience will be captured by interview after 4 weeks.	The users will be asked about the device's features and encouraged to provide general feedback about their experience. They will be asked if they believed they received active or comparator treatment.	4 weeks

Collaborators and Investigators

• Sponsor: Otivio AS
• Investigators: Principal Investigator: Peter Vestergaard Rasmussen, MD, PhD, Department of Clinical Medicine - The Department of Neurology, Aarhus University; Principal Investigator: Kjell-Morten Myhr, MD, PhD, Dept. of Neurology Haukeland Univ. Hospital & Dept. of Clin. Med., Univ. of Bergen, Bergen, Norway; Principal Investigator: Sara Haghighi Mobarhan Smith, MD, PhD, Department of Neurology, Motala Hospital, Motala, Sweden

Study record dates

Study Major Dates

• Study Start (Actual): October 4, 2022
• Primary Completion (Estimated): July 15, 2023
• Study Completion (Estimated): August 15, 2023

Study Registration Dates

• First Submitted: September 23, 2022
• First Submitted That Met QC Criteria: September 28, 2022
• First Posted (Actual): September 30, 2022

Study Record Updates

• Last Update Posted (Actual): June 29, 2023
• Last Update Submitted That Met QC Criteria: June 28, 2023
• Last Verified: June 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Nervous System Diseases; Immune System Diseases; Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Demyelinating Diseases; Autoimmune Diseases; Pain; Neurologic Manifestations; Musculoskeletal Diseases; Muscular Diseases; Neuromuscular Manifestations; Muscle Hypertonia; Multiple Sclerosis; Sclerosis; Chronic Pain; Muscle Spasticity
• Other Study ID Numbers: CIV-22-04-039306

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No