Upper Limb Tremor Reduction in Essential Tremor Patients

Encora, Inc.71 enrolled

Overview

This study is designed to demonstrate the safety, tolerability, and efficacy of the Encora Therapeutics Tremor Mitigation Device in subjects with upper limb tremor caused by Essential Tremor.

A prospective, randomized, blinded clinical trial. Subjects meeting all inclusion criteria will have five days of treatment with each of the three arms, received in a randomized order. Subjects will complete two rounds of assessments each day. Arm 1: Inactive stim Arm 2: Stim therapy utilizing a specific dermatome Arm 3: Stim therapy utilizing a tailored frequency

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

Conditions

Essential Tremor

Interventions

Encora Therapeutics Tremor Reduction DeviceDEVICE

The proposed therapeutic device uses vibration motors positioned around the wrist that provide on-demand-therapy to suppress resting, postural, or action tremors of the hand.

Eligibility

Sex: ALLMin age: 22 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion/Exclusion: Inclusion Criteria: 1. Between the ages of 22 and 80 years of age 2. A diagnosis of essential tremor (definite or probable based on TRIG criteria) 3. At least one hand exhibiting tremor \> 2 as assessed by the Essential Tremor Rating 4. Assessment Scale (TETRAS) finger to nose task, duck wing task, OR Archimedes Spiral completed during the Screening visit 5. Stable tremor medications for at least 30 days prior to enrollment and the ability to maintain stable medications through the duration of the study Randomization Inclusion Criteria 1. During the Baseline evaluation period, a median tremor score of \> 2 on at least one hand as assessed by the TETRAS finger to nose task, the duck wing task, OR the Archimedes Spiral AND 2. During the Baseline evaluation period, a median score of \> 3 on any one of the subject-assessed items of the Bain \& Findley Activities of Daily Living Scale (BF-ADL) Exclusion Criteria: 1. Previous surgical interventions for tremor reduction on the upper limb being used for inclusion in this study (eg, thalamotomy procedure, including Stereotactic Thalamotomy, Gamma Knife Radiosurgical Thalamotomy, or focused ultrasound) 2. Use of botulinum toxin for treatment to hand tremor within six months of enrollment 3. Suspected or diagnosed epilepsy or other seizure disorder 4. Other possible causes of tremor, including Parkinson's disease, drug-induced tremor, or dystonia 5. Pregnant 6. Swollen, infected, inflamed areas, or skin eruptions, open wounds, or cancerous lesions of skin at stimulation site 7. Numbness, tingling or pain affecting the tested upper extremity (eg, suspected or confirmed peripheral neuropathy, carpal tunnel syndrome) 8. Known allergy to silicone 9. Subjects are unable or unwilling to comply with the protocol requirements 10. Subject is part of a vulnerable population who is unable to give Informed Consent for reasons of incapacity, dementia, immaturity, adverse personal circumstances or lack of autonomy. This may include individuals with mental disability, persons in nursing homes, children, impoverished persons, persons in emergency situations, homeless persons, nomads, refugees, and those incapable of giving informed consent. 11. Vulnerable populations also may include members of a group with a hierarchical structure such as university students, subordinate hospital and laboratory personnel, employees of the Sponsor, members of the armed forces, and persons kept in detention.

Locations (1)

Encora Therapeutics

Cambridge, Massachusetts, United States

Outcomes

Primary Outcomes

Tolerability (Rate of Subject-Assessed Comfort with Stimulation)

The rate of subject-assessed comfort with stimulation, on a Subject Stimulation Tolerance Questionnaire as measured by % of patient who tolerated the treatment either none of the time, some of the time or all of the time.