TREATMENT OF ALCOHOL HANGOVER USING ELECTRICAL STIMULATION

Abstract

A method of reducing or eliminating alcohol hangover symptoms in an individual identified as experiencing an alcohol hangover is disclosed. The method includes positioning a non-invasive nerve stimulation device on the individual's wrist, wherein the electrodes of the non-invasive nerve stimulation device are in electrically conductive contact with skin at acupuncture point P6 of the wrist. The method also includes generating a stimulation signal and delivering the stimulation signal to the acupuncture point P6 of the wrist to reduce or eliminate one or more alcohol hangover symptoms in the individual. The alcohol hangover symptoms could include headache, nausea, retching, vomiting, fatigue, gastrointestinal distress, drowsiness/lethargy, problems concentrating, dry mouth, and dizziness.

Claims

1. A method of reducing or eliminating alcohol hangover symptoms in an individual identified as experiencing an alcohol hangover, said method comprising the steps of: positioning a non-invasive nerve stimulation device on the individual's wrist, wherein the electrodes of the non-invasive nerve stimulation device are in electrically conductive contact with skin at acupuncture point P6 of the wrist; generating a stimulation signal; and delivering the stimulation signal to the acupuncture point P6 of the wrist to reduce or eliminate one or more alcohol hangover symptoms in the individual; wherein the alcohol hangover symptoms are selected from the group consisting of: headache, nausea, retching, vomiting, fatigue, gastrointestinal distress, drowsiness/lethargy, problems concentrating, dry mouth, and dizziness.

2. The method of claim 1, wherein the stimulation signal comprises individual pulses at power levels of about 1-100 milliamps peak pulse height, at a pulse frequency of about 31 Hz +/10% such that there is a period of 32 msec between alternating monophasic pulses.

3. The method of claim 2, wherein the stimulation signal comprises individual pulses at power levels of about 1-50 milliamps peak pulse height at tolerances of 15%.

4. The method of claim 2, wherein the stimulation signal comprises individual pulses at power levels of about 1-40 milliamps peak pulse height at tolerances of 15%.

5. The method of claim 2, wherein the stimulation signal comprises individual pulses at power levels of about 8-40 milliamps peak pulse height at tolerances of 15%.

6. The method of claim 2, wherein the stimulation signal comprises individual pulses at power levels selected from the group consisting of: about 8 milliamps peak pulse height at tolerance of 15%; about 11 milliamps peak pulse height at tolerance of 15%; about 14 milliamps peak pulse height at tolerance of 15%; about 17 milliamps peak pulse height at tolerance of 15%; about 20 milliamps peak pulse height at tolerance of 15%; about 24 milliamps peak pulse height at tolerance of 15%; about 28 milliamps peak pulse height at tolerance of 15%; about 32 milliamps peak pulse height at tolerance of 15%; about 36 milliamps peak pulse height at tolerance of 15%; and about 40 milliamps peak pulse height at tolerance of 15%.

7. The method of claim 1, wherein the stimulation signal is delivered for 5-10 minutes or longer.

8. The method of claim 1, wherein the stimulation signal is delivered for 30 minutes or longer.

9. The method of claim 1, Wherein the stimulation signal is delivered for 60 minutes or longer.

10. The method of claim 1, wherein the stimulation signal is delivered for 90 minutes or longer.

11. The method of claim 1, wherein the stimulation signal is delivered for 120 minutes or longer.

12. The method of claim 1, wherein the stimulation signal is delivered for 150 minutes or longer.

13. The method of claim 1, wherein the stimulation signal is delivered for 180 minutes or longer.

14. The method of claim 1, wherein the stimulation signal is delivered for longer than 180 minutes.

Description

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0011] The biological effects of electrical stimulation of the P6 acupuncture point are more expansive than the suppression of nausea described in the Bertolucci patent. In addition to nausea, the methods described herein may be used to reduce or eliminate one or more additional alcohol hangover symptoms such as headache, nausea, retching, fatigue, gastrointestinal distress (e.g., vomiting and diarrhea), drowsiness/lethargy, problems concentrating, dry mouth, and dizziness in individuals who are experiencing an alcohol hangover. Such individuals may be identified as having a hangover by determining that the individual consumed alcohol and is experiencing symptoms of alcohol hangover. The individual may be treated with a device such as those set forth in U.S. Pat. Nos. 4,981,146, 6,076,018, 6,567,695, 6,735,480, 7,127,288, 7,171,266, 7,171,276, 7,983,761, or provisional application No. 62/614,212 entitled WEARABLE DEVICE FOR DELIVERING ELECTRICAL STIMULATION TO THE P6 ACUPUNCTURE POINT and filed Jan. 5, 2017. Such devices are used to apply electrical stimulation to the ventral side of the wrist (or the P6 acupuncture point or the median nerve). Any suitable means of applying electrical stimulation to the median nerve should work to relieve and eliminate symptoms associated with an alcohol hangover. Also, while the method generally uses the electrical stimulation to the median nerve at its superficial route through the wrist, stimulation of the median nerve along its entire course should provide similar benefits.

[0012] In some embodiments, the P6 electrostimulation device provided herein the pulse generation (output) of the device is as follows. Waveform may be asymmetrical balanced and biphasic. In some embodiments, the power level of the output is from 0.1 mA to 50 mA. In some embodiments, the power level of the output is from <1 mA. to 40 mA. In some embodiments, ten (10) intensity levels (defined by the maximum current amplitude measured at the peak of the stimulus pulse when unit is driving a 500 ohm purely resistive load) will be available (all expressed as setting level=output in milliamperes) are provided. In some embodiments, the ten intensity settings may be as follows: 1=8, 2=11, 3=14, 4=17, 5=20, 6=24, 7=28, 8=32, 9=36, 10=40, at tolerances of 15%. In some embodiments, amplitude to be nominally constant current (+/20% of output into 500-ohm load), is tested at 200 ohm and 1000 ohm loads. In some embodiments, amplitude may be automatically modulated using a 1 second ramp up to setting, 2 seconds constant at setting, 1 second ramp down to zero or lowest possible value, repeating continuously. In some embodiments, pulse width may be 350 seconds +/10%. In some embodiments, pulse frequency may be 31 Hz (32 msec period between alternating monophasic pulses) +/10%. In some embodiments, pulse waveform may be such that the ratio of: [pulse amplitude at 50+/2 seconds after the start of the pulse] to [peak pulse amplitude at start of pulse] may be equal to 0.51+/12%. In some embodiments, waveform will be such that the ratio of: [pulse amplitude at 100+/4 seconds after the start of the pulse] to [peak pulse amplitude at start of pulse] will be equal to 0.26+/20%. In some embodiments, the device may incorporate an output regulation feature such that the stimulation output amplitude does not vary more than 20% from the nominal as the battery charge decreases while in use. In some embodiments, the device may incorporate an automatic shut off feature such that when output regulation cannot be maintained for any setting, the device will shut off. In some embodiments, battery capacity and performance will deliver a minimum of 16 hours of continuous therapy from a full charge at intensity level 5 (which is half of the maximum output, or 20 mA output level) when tested using a 500 ohm purely resistive load.

[0013] In some embodiments, the overall waveform comprises a series of bipolar trapezoidal waveform that make low frequency pulses. The waveform is initiated at low power levels of about 1 to 2 volts and ramps up over a period of about 1 second to a maximum level of 17-18 volts, and is maintained for about 2 seconds, and then ramps down over a period of about 1 second to low power levels of about 1 to 2 volts. (The voltage specified is measured across a 500-ohm resistive load as suggested in ANSI/AAMI NS-4 (1986), American National Standard for Transcutaneous Electrical Nerve Stimulators.) The individual pulses are separated by about 31-32 milliseconds (msec)(measured peak to peak), and last about 350 microseconds (sec) power levels of about 1-100 milliamps peak pulse height, in some embodiments preferably 10-50 milliamps peak pulse height and in some embodiments 10-35 milliamps peak pulse height. A wide range of pulse patterns may be used in noninvasive nerve stimulation devices. The individual pulses alternate between negative and positive pulses, and are said to constitute a bipolar waveform. The individual pulse is made of a sharply vertical spike which decays exponentially over a period of about 350 sec, thus comprising a basically vertical leading edge and an exponentially decaying trailing edge to each individual pulse. The following pulse will be shaped the same, except that it will be of negative voltage. The exponential nature of the individual pulse decay maximizes the high frequency components in the signal. These high frequency components contribute to a lessening of the skin impedance, in particular the capacitive components. This contributes to a higher level of current able to enter the deeper tissues. The power levels may be adjusted up or down to intensify the therapeutic effect of the device or lessen the sensation causes by the device, according to the preferences of individual users. The pulse rate within the waveform may be increased or decreased also.

[0014] To use one of the devices such as those set forth in U.S. Pat. Nos. 4,981,146, 6,076,018, 6,567,695, 6,735,480, 7,127,288, 7,171,266, 7,171,276, 7,983,761, or provisional application No. 62/614,212 entitled WEARABLE DEVICE FOR DELIVERING ELECTRICAL STIMULATION TO THE P6 ACUPUNCTURE POINT and filed Jan. 5, 2017, to alleviate symptoms of alcohol hangover in a person experiencing an alcohol hangover, the user merely secures the device on their wrist positioning the electrodes over the P6 acupuncture point, in electrical contact with the skin overlying the median nerve. The user then turns the device on, adjusts it to a comfortable power level, and allows stimulation to continue for a few minutes, for example 5-10 minute or longer, in some embodiments 30 minutes of longer, in some embodiments 30 minutes of longer, in some embodiments 90 minutes of longer, in some embodiments 120 minutes of longer, in some embodiments 150 minutes of longer, in some embodiments 180 minutes of longer, in some embodiments longer than 180 minutes, to achieve relief. The device may be applied intermittently, once every hour or so, or continuously. The device provides electrical current and voltage to the electrodes to relieve symptoms of alcohol hangover in a person experiencing an alcohol hangover. The device will eliminate the symptoms entirely, or reduce them to more tolerable levels.

[0015] In a preferred embodiment, the P6 electrostimulation devices comprises pair of metal electrodes made of 316L stainless steel manufactured using metal injection molding technology that are substantially D-shaped, having a straight edge and an arcuate edge. The D shaped electrodes made of 316L stainless steel manufactured using metal injection molding technology are arranged such that when the device is properly worn by a user and the electrodes are in contact with the P6 point on a user's wrist, the straight edges of the electrodes oppose each other, i.e. arranged with the straight edges facing each other in apposition. The straight edges are thus parallel to each other. The electrodes are arranged on the device such that when the device is properly worn by a user and the electrodes are in contact with the P6 point on a user's wrist, the straight edges are perpendicular with the direction of the user's arm between the wrist and elbow. The straight edges have a length of about 1 inch, and the arcuate edges having an inner radius of about 0.5 inches. In a preferred embodiment, D shaped electrode is about 22.00 to about 25.50 mm and the arcuate edges having an inner radius of about 10.50 to about 13.00 mm. In a preferred embodiment, each D shaped electrode has a thickness of about 0.50 to about 1.75 mm. In a preferred embodiment, D shaped electrode is about 23.00 to about 24.50 mm and the arcuate edges having an inner radius of about 11.00 to about 12.70 mm. In a preferred embodiment, each D shaped electrode has a thickness of about 0.80 to about 1.40 mm. In a preferred embodiment, D shaped electrode is about 23.84+/0.10 mm and the arcuate edges having an inner radius of about 11.83+/0.10 mm. In a preferred embodiment, each D shaped electrode has a thickness of about 1.08+/0.10 mm.

[0016] The electrodes are arranged on the device such that the straight edges of the electrodes face each other in apposition and are separated by a gap. In some embodiments, the gap is 0.05 to 0.5 inches or 1-15 mm. in some embodiments, the gap is 0.1 to 0.25 inches or 2-7.5 mm. In some embodiments, the gap is 3-5 mm. In some embodiments, the gap is 0.14 inches.

[0017] In some embodiments, the D shaped electrodes are used in the P6 electrostimulation devices and the electrodes are connected to the electrical conduits that supply electrical output at a position on or immediately adjacent to, i.e. within 5 mm, preferably within 3 mm of the center point of the arcuate edge.

[0018] The extent that an individual is provided with relief from hangover symptoms, such relief may be complete or a reduction in severity. The relief of symptoms may extend to all symptoms or a subset. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including headache. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including fatigue. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including gastrointestinal distress. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including drowsiness/lethargy. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including problems concentrating. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including dry mouth. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including dizziness. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including nausea. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including retching. In some embodiments, the method of treatment to an individual experiencing a hangover may result in reduction or elimination of hangover symptoms including vomiting.

[0019] While the preferred embodiments of the methods have been described in reference to the environment in which they were developed, they are merely illustrative of the principles of the inventions. Other embodiments and configurations may be devised without departing from the spirit of the inventions and the scope of the appended claims.