Facial Function Reanimation by Electrical Pacing in Unilateral Facial Paralysis.
Primary Purpose
Facial Nerve Palsy
Status
Unknown status
Phase
Phase 1
Locations
Finland
Study Type
Interventional
Intervention
Electrical muscle stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Facial Nerve Palsy focused on measuring facial nerve palsy, facial paralysis, functional electrical stimulation, facial pacing
Eligibility Criteria
Inclusion Criteria:
- a unilateral peripheral facial nerve palsy (patients)
- willingness to participate (patients, healthy volunteers)
Exclusion Criteria:
- malignant diseases (a previously treated cancer is not an exclusion criterion)
- unstable cardiovascular disease
- severe immune deficiency
- other severe neurological diseases (causing cognitive or physical impairment)
- diabetic neuropathy
Sites / Locations
- Tampere University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Electrical stimulation
Arm Description
Outcomes
Primary Outcome Measures
Amplitudee of the movement elicited by electrical stimulation
The offline video analysis is done to determine the current threshold at which a movement of the target muscle is produced. Possible activations of the other muscles alongside the target muscle are also observed. The amplitude of the movement is analyzed offline from a video recording either visually by the investigators, or measured with a digital ruler. With visual evaluation, the outcome is measured on a rough level, i.e. whether the stimulated movement was larger in amplitude compared to the voluntary movement. With a digital ruler, the results a presented numerically (millimeters). The stimulated activation is compared to the voluntary activation of the muscle. Further, in some sub-studies, the facial activations are evaluated with the Facial Action Coding System.
Secondary Outcome Measures
Subjective ratings related to the tolerability of stimulations
The participants evaluate the experienced discomfort and painfulness of the stimulation with a numeric rating scale (NRS).
Subjective ratings related to acceptability of the stimulated movement
The participants evaluate the naturalness and symmetry and their satisfaction with the stimulation elicited movement with an NRS.
Visual acuity
In substudies concerning the elicitation of eye blink, The visual acuity is measured for both eyes separately with a LogMAR chart before and after the stimulation session.
Changes in lacrimal fluid
In substudies concerning the elicitation of eye blink, a lacrimal fluid sample is collected before and after the stimulation session to investigate the possible effects of the stimulation in its constitution.
Full Information
NCT ID
NCT03496025
First Posted
March 19, 2018
Last Updated
December 17, 2020
Sponsor
Tampere University Hospital
Collaborators
Tampere University, Tampere University of Technology, Helsinki University Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03496025
Brief Title
Facial Function Reanimation by Electrical Pacing in Unilateral Facial Paralysis.
Official Title
Mimetic Interfaces - Toispuoleisen Kasvohermohalvauksen Kojeellinen Kuntoutus Terveen Puolen Lihasaktiviteettiohjauksella. Stimulaattorin Prototyypin Testaus terveillä koehenkilöillä ja Kasvohermohalvauspotilailla.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2015 (Actual)
Primary Completion Date
October 31, 2018 (Actual)
Study Completion Date
May 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tampere University Hospital
Collaborators
Tampere University, Tampere University of Technology, Helsinki University Central Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Purpose of the trial is to study the activations of paralyzed facial muscles in a unilateral facial nerve palsy with a multi-channel electrical stimulator. The principle of the device is to measure muscle activity of the healthy side of the face by surface electromyography (EMG) and to use this information to stimulate the corresponding muscles of the paralyzed side. The ultimate goal is to develop a prosthetic device for persons with a facial nerve palsy.
The trial consists of several different studies. The studies' aims are 1. To study activations of paralyzed facial muscles by the electrical stimulation. 2. To study different stimulation pulse waveforms, frequencies, and electrode placement and their effect on the muscle activations and the tolerability of the stimulation. 3. To study whether a symmetrical movement on the paralyzed side can be achieved with electrical stimulation when compared to the movements of the healthy side. 4. To study tolerability of stimulation-elicited eye blink when watching a film and the effect of the stimulation-induced blink on the eye symptoms, the visual acuity, and the effects of the stimulation on the lacrimal fluid. 5. To develop a method for facial pacing, i.e. measuring the muscle activations on the healthy side of the face and to use this information to stimulate and activate the healthy side of the face.
Forty subjects with a chronic facial nerve palsy are recruited to the studies. Each subject can participate in one or several studies. Another forty subjects with an acute facial nerve palsy are recruited to the study on the tolerability and effect on the eye symptoms. Additionally, altogether ninety healthy volunteers are recruited to the studies in order to gather preliminary information on the tolerability and the effects of the stimulations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Facial Nerve Palsy
Keywords
facial nerve palsy, facial paralysis, functional electrical stimulation, facial pacing
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
77 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Electrical stimulation
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Electrical muscle stimulation
Intervention Description
The intervention consists of activating paralyzed facial muscles with electrical stimulation.
Primary Outcome Measure Information:
Title
Amplitudee of the movement elicited by electrical stimulation
Description
The offline video analysis is done to determine the current threshold at which a movement of the target muscle is produced. Possible activations of the other muscles alongside the target muscle are also observed. The amplitude of the movement is analyzed offline from a video recording either visually by the investigators, or measured with a digital ruler. With visual evaluation, the outcome is measured on a rough level, i.e. whether the stimulated movement was larger in amplitude compared to the voluntary movement. With a digital ruler, the results a presented numerically (millimeters). The stimulated activation is compared to the voluntary activation of the muscle. Further, in some sub-studies, the facial activations are evaluated with the Facial Action Coding System.
Time Frame
Immediate
Secondary Outcome Measure Information:
Title
Subjective ratings related to the tolerability of stimulations
Description
The participants evaluate the experienced discomfort and painfulness of the stimulation with a numeric rating scale (NRS).
Time Frame
Immediate
Title
Subjective ratings related to acceptability of the stimulated movement
Description
The participants evaluate the naturalness and symmetry and their satisfaction with the stimulation elicited movement with an NRS.
Time Frame
Immediate
Title
Visual acuity
Description
In substudies concerning the elicitation of eye blink, The visual acuity is measured for both eyes separately with a LogMAR chart before and after the stimulation session.
Time Frame
Immediate
Title
Changes in lacrimal fluid
Description
In substudies concerning the elicitation of eye blink, a lacrimal fluid sample is collected before and after the stimulation session to investigate the possible effects of the stimulation in its constitution.
Time Frame
Immediate
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
a unilateral peripheral facial nerve palsy (patients)
willingness to participate (patients, healthy volunteers)
Exclusion Criteria:
malignant diseases (a previously treated cancer is not an exclusion criterion)
unstable cardiovascular disease
severe immune deficiency
other severe neurological diseases (causing cognitive or physical impairment)
diabetic neuropathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Rautiainen, MD, PhD
Organizational Affiliation
professor, head physician
Official's Role
Study Director
Facility Information:
Facility Name
Tampere University Hospital
City
Tampere
ZIP/Postal Code
33521
Country
Finland
12. IPD Sharing Statement
Citations:
PubMed Identifier
33438658
Citation
Makela EA, Ilves MK, Venesvirta HM, Lylykangas JK, Rantanen VT, Vehkaoja AT, Verho JA, Lekkala J, Surakka VV, Rautiainen MEP. Effect of pulse waveforms on movement amplitudes and perceived discomfort in electric muscle stimulation in unresolved facial nerve palsy. Biomed Phys Eng Express. 2020 Mar 25;6(3):035013. doi: 10.1088/2057-1976/ab7eea.
Results Reference
derived
Learn more about this trial
Facial Function Reanimation by Electrical Pacing in Unilateral Facial Paralysis.
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