Energy stimulated acupuncture, directed to a novel set of acupoints, is implemented to treat hypertension. Methods and systems apply electrical stimulation, or other forms of energy, to specific acupuncture points, using devices such as transcutaneous electrical stimulation electroacupuncture devices, laser acupuncture devices or ultrasound acupuncture devices, to treat hypertension, particularly in middle-aged women.

A kit for discharging electrons from a human comprises at least two electrically conductive electrodes. The electrodes are adapted for creating an electrical connection with skin of the human. There is an electrically conductive pad with electrically conductive pad wires, one for each electrode for connection to the respective electrode to the pad. Electrically conductive grounding wire is provided for electrically grounding the pad. The kit can comprise electrically conductive gel for use with the electrodes to enhance electrically conductivity. The kit is designed, when assembled and used to treat a human, for withdrawing excess electrons from the human for improved health.

A microneedle skin care device includes a housing having a predetermined space formed therein; a sound wave module disposed inside the housing to provide sound wave vibration; a microneedle assembly configured to receive vibration of the sound wave module and vibrate in front and rear directions, the microneedle assembly having microneedles disposed at a front end; and a needle tip coupled to the front end of the microneedle assembly and having through-holes through which the microneedles selectively pass through formed corresponding to the microneedles.

A microneedle skin care device includes a housing having a predetermined space formed therein; a sound wave module disposed inside the housing to provide sound wave vibration; a microneedle assembly configured to receive vibration of the sound wave module and vibrate in front and rear directions, the microneedle assembly having microneedles disposed at a front end; and a needle tip coupled to the front end of the microneedle assembly and having through-holes through which the microneedles selectively pass through formed corresponding to the microneedles.

The present invention relates to a negative pressure device, including: a hollow needle assembly including: a hollow needle adaptor, the hollow needle adaptor has an axial through hole, a proximal connector, a distal connector and a flange between the proximal connector and the distal connector, and at least one hollow needle, each of the at least one hollow needle has a tip and an axial through hole and is in fluid communication with the proximal connector of the hollow needle adaptor; a host machine, the host machine includes a control module and a vacuum pump; and an exhaust pipe, the exhaust pipe is in fluid communication with the host machine and the distal connector of the hollow needle adaptor.

This implantation device includes: a set of separable implants, a guide member defining a passage for guiding the set of implants in translation towards the outlet orifice, a transmission member for transmitting a pushing force in order to move the set of implants towards an outlet, the transmission member having several successive projections, and a pushing member to allow the practitioner to generate the pushing force. The pushing member includes a bearing part configured to bear against several of the projections during successive movements of the pushing member, the bearing part having in succession a bearing position and a clearing position, and a unidirectional stop element connected to the guide member and configured to have in succession i) a configuration of clearance by a projection and ii) a stop configuration so as to immobilize the transmission member in the inverse direction of the translation towards the outlet.

This implantation device includes: a set of separable implants, a guide member defining a passage for guiding the set of implants in translation towards the outlet orifice, a transmission member for transmitting a pushing force in order to move the set of implants towards an outlet, the transmission member having several successive projections, and a pushing member to allow the practitioner to generate the pushing force. The pushing member includes a bearing part configured to bear against several of the projections during successive movements of the pushing member, the bearing part having in succession a bearing position and a clearing position, and a unidirectional stop element connected to the guide member and configured to have in succession i) a configuration of clearance by a projection and ii) a stop configuration so as to immobilize the transmission member in the inverse direction of the translation towards the outlet.

A wearable stimulator device can be used to treat nausea and vomiting resulting from pregnancy, gastroparesis, virtual reality use, motion sickness, chemotherapy, and post-surgical nausea and vomiting, or other conditions by stimulating the P6 point of a user's forearm. A method of treating nausea includes monitoring one or more physiological parameters of a user via a wearable device, for example a smartwatch. Based on the one or more physiological parameters, the P6 point of the user's forearm can be stimulated for a predetermined time, for example via vibrational stimulation effected via a smartwatch or other wearable device. Data regarding the user's physiological parameters, stimulation sessions, and user-provided input regarding treatment efficacy and user symptoms can be collected and analyzed at scale to develop improved treatment regimes, for example modifying stimulation waveforms and/or timing, and identifying physiological parameters useful for predicting the onset of nausea.

A method is provided for a novel application of trigger point dry needling. A target tissue is identified based on the observation of a series of movement patterns performed by the patient. Once identified, a needle movement protocol is used to insert a needle into the target tissue to a myofascial trigger point during one or more movement patterns. The needle protocol is adjusted until a local twitch response is induced.

A method is provided for a novel application of trigger point dry needling. A target tissue is identified based on the observation of a series of movement patterns performed by the patient. Once identified, a needle movement protocol is used to insert a needle into the target tissue to a myofascial trigger point during one or more movement patterns. The needle protocol is adjusted until a local twitch response is induced.