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Bridge is the first FDA-cleared, drug-free, non-surgical device to use neuromodulation to aid in the reduction of symptoms associated with opioid withdrawal.
In a study of 73 adult patients with opioid use disorder, a reduction in opioid withdrawal symptoms was observed when Bridge was used during active withdrawal. The study demonstrated Bridge to be:
Help users successfully progress in treatment:
Bridge is a small electrical nerve stimulator device that contains a battery-powered chip and wires that are applied around a patient's ear. It requires a prescription and is offered to qualified healthcare professionals with training. Bridge includes a kit containing everything required to apply the device.
Bridge can be used for patients* experiencing opioid withdrawal symptoms, while undergoing treatment for opioid use disorder when:
References:
*Contraindications: Use of cardiac pacemakers, Hemophilia, Psoriasis vulgaris
1Miranda A, Taca A. Neuromodulation with percutaneous electrical nerve field stimulation is associated with reduction in signs and symptoms of opioid withdrawal: a multisite, retrospective assessment [published correction appears in Am J Drug Alcohol Abuse. 2018;44(4):498]. Am J Drug Alcohol Abuse. 2018;44(1):56‐63. doi:10.1080/00952990.2017.1295459
2Roberts, Arthur et al. “Minimal adverse effects profile following implantation of periauricular percutaneous electrical nerve field stimulators: a retrospective cohort study.” Medical devices (Auckland, N.Z.) vol. 9 389-393. 3 Nov. 2016, doi:10.2147/MDER.S107426Roberts, Arthur et al. “Minimal adverse effects profile following implantation of periauricular percutaneous electrical nerve field stimulators: a retrospective cohort study.” Medical devices (Auckland, N.Z.) vol. 9 389-393. 3 Nov. 2016, doi:10.2147/MDER.S107426.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. See instructions for use for full prescribing information, including indications, contraindications, warnings, and precautions.
PLCO-005805/PLM-12507C-0322