The complex is destined for the treatment of vision disturbances by means of transcutaneous electric stimulation of the optic nerve and the eye retina.


1. Optic nerve atrophy caused by:

  • pregnancy and childbirth pathologies leading to hypoxia or brain trauma of a child (toxicoses, abortion threat, various gynecopathies during pregnancy, birth traumata), perinatal life diseases;
  • inflammatory processes (meningitis and meningoencephalitis of various genesis);
  • opticochiasmal arachnoiditis;
  • disseminated sclerosis (disseminated encephalomyelitis);
  • craniocerebral injury, eyeball damage;
  • hypertension syndrome (of non-tumor genesis);
  • chiasmal-cellar area brain tumors or tumors of another localization (after the tumor removing only);
  • vascular disorders (hypertension, atherosclerosis, cerebral strokes);
  • glaucoma (with compensated intraocular pressure only);
  • toxic factors (including methyl alcohol intoxication).

2. Retina pathologies:

  • pigmentary degeneration (tapeto-retinal abiotrophia);
  • central degeneration (Shtargardt youthful type, Kurt-Unius senile type, sclerotic maculodistrophy);
  • chorioretinites of various genesis;
  • diabetic angiopathy (insular diabetes).

3. Myopia (including myopic chorioretinitis), amblyopia.

4. Accommodation spasm, display disease (the vision weakening caused by continuous work at a computer).

А treatment course is carried out continuously for 10 - 15 days, with 10…30 minutes a day.

Considerable improvement of vision can be observed not only during the treatment course, but in 3…4 months later also. Further improvements can be achieved by repeating the treatment courses in 5…6 months.


  • Multichannel automatic transcutaneous stimulation by means of a multizone eye electrode.
  • Type of electric stimulus: periodic sequence of bipolar rectangular current pulses with controllable amplitude, frequency, and duration. The pulses are grouped into packets, series, and cycles.  
  • Ability for automatic frequency variation during the stimulation by periodic or random law (frequency swinging).
  • Mapping a diagram of actual stimulus parameters (current and voltage values) for each stimulated zone.
  • Complex body impedance measuring for each stimulated zone both in stimulus intensity setting and stimulation modes.
  • Mapping the dynamics of actual complex body impedance for each stimulated zone.
  • Use of preset (typical) stimulus parameters values or manual setting the desirable values.
  • The hardware module is powered by the computer accumulator.