Basic Assessment of Safety and Minimally Invasive Stimulation Via Injectrode

NCT ID: NCT04672096

Last Updated: 2024-04-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-12-04
• Study Completion Date: 2021-05-21

Brief Summary

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.

Detailed 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.

Conditions

Chronic Lower Limb Pain

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DEVICE_FEASIBILITY
• Blinding Strategy: NONE

Study Groups

Neuronoff BASMATI Injectrode

Subjects will be provided with the placement of an Injectrode insert. The maximal placement duration will be 28 days.

Group Type: EXPERIMENTAL

Neuronoff BASMATI Injectrode

Intervention Type: DEVICE

The 28 day temporary placement of a Basmati Injectrode does not result in unexpected levels of inflammation or encapsulation.

Interventions

Neuronoff BASMATI Injectrode

The 28 day temporary placement of a Basmati Injectrode does not result in unexpected levels of inflammation or encapsulation.

Intervention Type: DEVICE

Other Intervention Names

Injectrode; BASMATI Injectrode

Eligibility Criteria

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).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Ohio Pain Clinic

OTHER

Sponsor Role: collaborator

Neuronoff, Inc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Amol Soin, MD

Role: PRINCIPAL_INVESTIGATOR

Ohio Pain Clinic

Locations

Ohio Pain Clinic

Dayton, Ohio, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

NCP-01

Identifier Type: -

Identifier Source: org_study_id