Swallowed Microprocessor Capsule
Autonomous Electrostimulator of Gastrointestinal Tract
and Mucous Membranes
(AES GIT & MM)
"Electronic Normalizer"
The name "Electronic Normalizer" is given by the Committee for New Technology,
Russian Federation Ministry of Health Protection and Medical Industry
(Protocol No. 6 dated July 11, 1995).
MO2.B02388).
943115.002).
Article AES GIT & MM "Electronic Normalizer" (hereinafter, EN) (Patent "Electronic stimulator" No 1632 dated 28.12.93, Patent "Electronic normalizer" No 2071368 dated 30.01.96, International Patent "Electronic normalizer" PCT/RU/00023 dated 31.01.96), is a complex electronic device assigned for correction of disorders in the organism from the cells to the system level. At the same time, the normalizing effect is unprecedented in duration and cannot be achieved by other means of medicine. The positive effect is provided by a complex of the following factors:
The great amount of investigations, works, and tests enabled the ECOMED Research and Production Association to use articles "Complex-1" (1969) and AES GIT (1984) as the basis for designing a rather perfect article AES GIT & MM "Electronic Normalizer" (1991), which is able to use all the factors aforementioned for complex influence on the organism. This article is permanently improved.
In accordance with the estimates of foreign and home specialists of health protection, EN is an instrument of the new class of apparatuses, which enable without any medicaments, traumas, allergies and beyond clinical conditions with independently available periodicity to perform effective correction and activation of the whole series of disordered systems of the organism.
The undoubtedly positive effect of EN on the organism includes desintoxication of the organism, its decontamination from slags and diffuse depositions, regeneration of working capacity of the whole gastrointestinal tract (GIT) and effectivestimulating effect on the adjacent organs through the mucosa.
The weak energy effect, unlike other methods of electrostimulation, provides a prolonged positive effect because it does not produce any suppressing influence on the biological systems but only activates and synchronizes their functioning. The weak secondary electromagnetic field, which is induced in electroconducting media of the organism, and the electrical signal affect the nervous system and change the concentration of neurohormones thus resulting in the prolonged change in the status of organs and systems of the organism and increase in their adaptation readiness.
Description:
The EN articles of all the types are hermetically sealed capsules consisting of two hemispheres, which serve simultaneously as electrodes and antenna vibrators suitable for swallowing (size is under 11 mm in diameter and 22 mm in length, weight is under 15.5 g). The capsule contains inside a microprocessor with devices for starting and provision of continuous operation in the case of shorting and the effect of static charge and a power source.
EN in packing is switched off and is automatically switched on when introduced in the electrolytic medium of the organism.
The capsule is shock-proof. It can be stored at an ambient temperature. The period of validity is up to one year (specified on the label).
The time of continuous work is over 50 hours.
Methods of administration:
Indications to application :
Medical:
The statuses aforementioned are indicated by the following effects:
Contraindications:
Mechanical intestinal obstruction, cicatrical stenoses.
Each indication to application is certified by the protocols of clinical tests performed in accordance with the programs approved by the ECOMED Research and Production Association using the improved AES GIT & MM - "EN" capsules produced by the ECOMED Research and Production Association by the leading clinics, medical institutes, and centers of the Russian Federation Ministry of Health Protection and Medical Industry, Russian Academy of Medical Sciences, and Ministry of Defense.
Please, do not confuse with articles AES GIT (11 MO.089.331 Technical Instruction) permissible for application only in clinical surgery. |
ADMINISTRATION MODES:
FIRST MODE (BASIC): Swallowing as a common medicament for electrostimulation of all the sections of gastrointestinal tract. EN is swallowed as a common tablet, it may be taken with water. EN causes the swallowing reflex and is swallowed easily. In some case, an acid taste in the mouth is noted that results from the electrical action of the electrostimulator upon switching on. It is recommended to perform the first swallowing in the morning of a day-off, because the patient has to get used to new feeling.
In 20 to 40 minutes after swallowing, some patients may show short spontaneous contractions of muscles of abdomen and legs that repeat periodically for 3 to 6 hours and do not produce any effect on working capacity. However, it is desirable to avoid driving a car in the first day after swallowing. In the first swallowing, some patients may feel no stimulator in the organism that depends upon the individual sensitivity and the degree of intestinal contamination.
Appearing in mucosa, EN affects it together with the adjacent organs with the specific complex impulse pseudopulse signals repeated periodically that causes contraction of peristaltic muscles and, in the case of atonia and intestinal paresis,increases the electrical activity of peristaltics including the sections with paresis. Meanwhile, in the sections with enhanced paresis, EN retards its movement and produces the maximum positive effect. The response of the organism in the form of peristaltic wave moves EN to distal sections. As EN moves it stimulates not only all parts of gastrointestinal tract but also adjacent organs by staged and consistent.
Even a single administration of EN results in the increase in secretory activity of female and male genitals, clears billary ducts and the duct system of prostate (for males). Generally, many male patients show strengthening of erection when EN passes the large intestine and rectum and increase in sexual activity within three days after EN leaves the organism. In particular, these effects are observed for patients with excess weight and obesity.
The average time of AES GIT & MM staying in a human organism equals 24 to 36 hours (minimum 5 hours and maximum 11 days).
EN is excreted from the organism by the natural way together with feces. While wastes and slags are excreted from the organism, some patients observe release of gases with unpleasant smell and changed colour of feces.
After leaving the organism, one of electrode hemispheres of EN may show darkened and stained surface. This is the result of electrochemical interaction of EN with acid or basic media of the organism.
ATTENTION! In the swallowing mode, each capsule is used ONLY ONCE, because its resource and external cover are exhausted almost completely when passing the intestines.
SECOND MODE: Isolated rectal electrostimulation (administration like rectal suppositories) in the case of wide intestinal paresis, stasis of large intestine and for the patients with preternatural anus. It is effective for activation of sexual function of male patients with chronic prostatitis.
In wide intestinal paresis, if the first mode was insufficient to eliminate constipations, it is recommended to swallow the capsule with simultaneous isolated stimulation of the large intestine and rectum. In this case, one capsule is swallowed and, in five to six days, the second capsule is introduced in rectum. The patient must lay on side, draw his knees to chest and introduce EN, which is preliminarily lubricated with any vegetable oil, into anus to the depth of the forefinger. After administration, it is recommended to lie for 30 to 40 minutes. After the procedure, the capsule is removed by muscular force, washed with soap and water or with alcohol and packed. The course included 5 to 15 rectal procedures every other day.
The general period of continuous operation of the normalizer equals at least 50 hours, therefore, a single capsule is sufficient for one or two course of electrostimulation per rectum. However, it should be taken into consideration that EN after leaving the organism is active until dry (for about 30 minutes).
In order to achieve the maximum effect, it is recommended to use this mode four or five times a year with the interval of two to three months.
For the patients with preternatural anus, it is recommended for evacuation of intestines to introduce the electrostimulator into the preternatural anus every two or three days. Strengthening of motor system of intestines is observed in 20 to 40 minutes after introduction. The course of 10 to 20 procedures is repeated in two or three months.
For activation of sexual function of male patients, it is recommended to use the therapeutical course of 10 to 20 procedures of 30 to 60 minutes every day with the interval of two or three months. In the case of preliminary washing the intestines with a small amount of water (150 to 300 g), the effect increases, but EN may be retained in the intestines for a day. In this case, electrostimulation of reflexogenic zones (release of blockade and regeneration of sensitivity of the semen tubercle of prostate causes excitation of the receptor center on prostate, improves blood circulation, produces the antiinflammatory effect, promotes the expressed stimulation of spinal centers of erection and ejaculation, and regenerates the sexual function.
Complex effectiveness is increased because of simultaneous restoration of volume of prostate channels and its activation by electric signal.
The ECOMED Research and Production Association performs manufacture and development of instruments AES GIT & MM "Electronic Normalizer" for different purposes, including:
Please, be careful: in the market, you can find counterfeits distributed with labels containing indications for use that are related only to the EN articles manufactured by the ECOMED Research and Production Association and accompanying documents on the tests performed with the EN articles.
Only articles AES GIT & MM - EN manufactured by the ECOMED Research and Production Association (in accordance with Technical Instruction 9444-014-11555014-95 and the MASI design documentation 943115.002) passed the following technical and medical tests (corresponding to the WHO requirements): toxicology for all the internal media, toxicology of the EN articles with galvanic coating, gastroenterology in ulcers and colitis, endocrinology, sexual pathology, psychiatry, neurology, immunology, oncology, extreme effects, and military indications. Only articles manufactured by the ECOMED Research and Production Association were supplied to the 4th Chief Department of Ministry of Health and are supplied to the institutions of the Government and the State Duma. |
