Infrared Neural Stimulation (INS) Clinical Trial
Official title:
Clinical Safety and Efficacy of Infrared Neural Stimulation During Nerve Transfers
Many surgical procedures such as brachial plexus reconstruction, nerve repair, and dorsal root rhizotomies rely on the spatial selectivity of their neural stimulation methods to identify specific nerve fascicles or rootlets. Due to the variable distribution of nerves between patients, many times it is not enough to rely on the historical topography of nerves to determine their location and identity.Currently, electrical stimulation (ES) methods are used to stimulate nerves in order to locate and map them intraoperatively. ES, however, is subject to current spread in which the electrical stimulus extends beyond the area proximal to the electrode into the surrounding tissue. This can result in the stimulation of multiple fascicles introducing ambiguity as to the location and/or identity of a specific nerve or fascicle. Our group has shown that infrared neural stimulation (INS), a novel optical and label-free means of exciting neural tissue, is capable of safely stimulating nerves with a higher degree of spatial specificity than traditional ES methods. Our clinical studies have even shown that INS can outperform ES, achieving isolated rootlet responses. The investigators hypothesize that the spatial selectivity of INS can be further utilized in upper extremity surgeries such as brachial plexus reconstruction and nerve transfers to improve intraoperative nerve identification and localization. While the initial clinical work was performed with a costly clinical laser system, our group has demonstrated the efficacy of cost-effective laser diode systems for INS in animal models in vivo.The safety of these lasers, however, has yet to be proven histologically in human patients. The objective of this proposal is two-fold: to demonstrate the efficacy of INS for spatially selective nerve stimulation in the upper extremity and to determine the histological safety of INS using diode laser systems in human patients. To do so, the investigators will recruit patients undergoing brachial plexus reconstruction (BPR) and nerve transfer surgeries wherein both the effectiveness and spatial selectivity of INS can be demonstrated and histological samples can be obtained without detriment to the patients' quality of care or recovery. To accomplish these objectives, the investigators propose the following aims: Aim 1: Design and fabricate a clinical fiberoptic probe for a diode-based INS system Aim 2: Demonstrate the efficacy of INS in nerve transfer cases Aim 3: Determine the histological safety of the diode-based INS system
| Status | Not yet recruiting |
| Enrollment | 12 |
| Est. completion date | January 1, 2026 |
| Est. primary completion date | July 1, 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria - Patient set to undergo a brachial plexus reconstruction or nerve transfer surgery - 18 years or older Exclusion Criteria - Patients under the age of 18 - Patients who are unwilling to take part in study - Patients who have documented psychiatric disorder that limits ability to consent - Patients who do not speak English - Patients who are pregnant |
| Country | Name | City | State |
|---|---|---|---|
| United States | Vanderbilt Department of Orthopaedic Surgery | Nashville | Tennessee |
| Lead Sponsor | Collaborator |
|---|---|
| Vanderbilt University Medical Center |
United States,
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* Note: There are 33 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Stimulation threshold | The stimulation threshold (H100) will be defined as the radiant exposure at which 100% of the laser pulses evoked CMAP responses and will be used to compare all data. To determine the stimulation threshold, recordings from each trial will be analyzed to determine the number of INS-evoked CMAPs. The number of evoked CMAPs will be divided by the total number of delivered pulses to determine the activation probability for every radiant exposure. | Day of surgery | |
| Primary | Transition rate | The transition rate to 100% activation probability will be defined as the peak slope of the fitted CDF (mpeak). This represents how well-defined the stimulation threshold is. For instance, a more immediate transition from 0 to 100%, a greater mpeak, corresponds to every pulse going from 0% to 100% activation over a small range of radiant exposures. Practically, a sharper transition rate translates to more reliable and predictable stimulation. Changes in peak CDF slope will then be compared across conditional groups. | Day of surgery |