Basic Assessment of Safety and Minimally Invasive Stimulation Via Injectrode (BASMATI)

Neuronoff

Status

Completed

Conditions

Chronic Lower Limb Pain

Treatments

Device: Neuronoff BASMATI Injectrode

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT04672096

NCP-01

Details and patient eligibility

About

The objectives of this non-significant risk (NSR) study are to evaluate the safety of the short term placement of the Basmati Injectrode for up to 28 days and the efficacy of conducting electrical current to stimulate subcutaneous nerves on the explant date just prior to explant.

Full description

This was a prospective, single-center, single-arm, non-randomized study design. A sample of 10 study participants were enrolled into the study, and provided with the placement of a Basmati Injectrode insert with a maximal placement duration of up to 28 days. Subjects who were selected to participate in the trial were healthy volunteers adults with ages 18 years and older without any preexisting condition indicated for treatment. Each subject was followed during the trial period of approximately 45+/-2 days.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Sign a valid, Institutional Review Board (IRB)-approved informed consent form (ICF) and understand the study requirements.
Be 18 years of age or older when written informed consent is obtained.
Be in good physical and mental health as assessed by a general practitioner.
Be able to tolerate electrical stimulation (TENS).
Be willing and able to understand and comply with all study-related procedures during the course of the study.

Exclusion criteria

Have a cognitive impairment or exhibit any characteristic that would limit the study candidate's ability to completely understand and sign a valid, IRB-approved informed consent form.
Have a positive pregnancy test (conducted during enrollment).
Have a positive Allergic reactivity to Gold skin test (conducted during enrollment).
Show symptoms indicative for Covid19 as assessed during enrollment.
Have a skin condition at the planned surgical location.
Have a blood coagulation disorder or other indication with the potential to impact the study biocompatibility data in unpredictable ways.
Have a medical condition that is a contraindication for minimally invasive surgery.
Be implanted with a cardiac defibrillator or pump.
Have a history of cardiac arrhythmia with hemodynamic instability
Be implanted with a neurostimulator.
Have any active electrical implant of any other kind.
Have metal implants (particularly in hip).
Have active infection.
Have allodynia.
Take regular use of antiplatelet medications (e.g. aspirin, ticlopidine (Ticlid), clopidogrel (Plavix), tirofiban (Aggrastat) or eptifibatide (Integrilin)).
Have untreated drug habituation or dependence.
Have uncontrolled seizures (averaging > 2 seizures per month).
Currently require, or be likely to require, diathermy and/or MRI during study duration.
Have a history of adverse reactions to local anesthetics (e.g. lidocaine).