Clinical Case Study

1. In Oct of 2003 and ISHRS.org Press Release regarding clinical study results of an LHT hand held device submitted to the FDA. Dr. Martin Unger of Toronto reported. The results were summarized:

      1. 100% of men had stabilization of hair loss in frontal and vertex (top of the head) areas;
      2. 84.6% of men had hair re-growth (11% of more from baseline) in the frontal area;
      3. 82.8% of men had hair re-growth (11% or more from baseline) in the vertex area;
      4. 87.5% of women had stabilization of hair loss in the frontal area;
      5. 100% of women had stabilization of hair loss in the vertex area;
      6. 75% of women had hair re-growth (11% or more from baseline) in the frontal area; and,
      7. 96.4% of women had hair re-growth (11% or more from baseline) in the vertex area.

Reference

2. In February of 2010, the FDA accepted and approved a laser hair therapy device company’s clinical study results which, in summary, reported subject results.

  1. 97% demonstrated an increased hair count of 20%
  2. 89% demonstrated an increased hair count of 30%
  3. 57% demonstrated an increased hair count of 50%

Reference

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FDA Registered Cosmetic Device
Nutreve Personal Hair Therapy Laser is a Class 3r Cosmetic Device. Not intended for medical use.