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"dense-packing" and "One-session-philosophy"

The success and quality of a hair transplantation are largely decided by the hair density of the transplanted hairs.

read more >

Mega-dense-packing
LINKS
www.hairtransplantnetwork.com
www.iahrs.org

www.ishrs.org

www.eshrs.org
www.propecia.com
(finasteride)
www.xandrox.com
(minoxidil)
www.vitrichol.com
www.aestheticclinics.com


PROPECIA®


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In nine out of ten cases, increasing hair loss is genetically determined. Partially responsible for the baldness is the so-called Dihydrotestosterone, in short DHT. This is formed with the help of an enzyme (the 5-alpha-reductase) from the male hormone testosterone.

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The effect of DHT to the hair roots

DHT influences the shortening of the growth phase of the hair. Furthermore, the hair root can observed to mortify and there can be an increase in the number of so-called downy hairs.

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How does PROPECIA® work?

The discovery of the 5-alpha-reductase enzyme reveals new treatment possibilities. If one succeeds in retaining the enzyme and suppress it, it is possible for a man to treat his genetically determined loss of hair by use of medication.
To be clear: PROPECIA does not take action in the hormonal regulation! The male hormone testosterone is not influenced by PROPECIA! PROPECIA merely stops the effect of the 5-alpha-reductase enzyme and by doing so, it lowers the concentration of DHT in the scalp.
In this way, PROPECIA helps to discontinue the progressive mortification of the existing hair roots. Hair roots that have already mortified are stimulated to produce sturdy hairs again.
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Possible side-effects

As the Dutch saying goes: "Wash me, but don't make me wet!". We all know that this is an unattainable desire, and this also goes for many forms of medication.
All medication can also have side-effects, beside the positive, desired effect.
The development of e100
ffective substances is now always goal-oriented, so that side-effects can be reduced. In the clinical research, only 3.8% of all males complained about sexual side-effects which are connected to the intake of PROPECIA (see also the report of clinical research).
These side-effects certainly took place during the treatment period and were only temporary or disappeared after stopping the intake of PROPECIA.

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The use of PROPECIA

In general, a daily tablet intake is required for a period of three to six months, before the effects of it become visible.
In order to maintain this effect optimally, PROPECIA needs to be used durably.
Because of this, a regular check-up by your physician is required. There are several persistent assumptions, which are untrue in all cases:

· Hair that has been cut short does not grow faster than long hair
· thin, fine hair does not become thicker by cutting it regularly
· hair roots cannot be stimulated by the use of vitamins
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Report of clinical studies

Three clinical studies found place with 1879 males in the ages of 18 to 41 years with finasteride 1 mg (PROPECIA®). The males in this studies with mild to moderate, but not complete, hair loss.
Two of these studies researched hair loss of the vertex, and the third study researched hair loss at the frontal and the middle part of the scalp.
In the studies of hair loss of the crown, 86% of men treated with finasteride suffered no further hair loss, or even experienced an increase of the number of hairs. In only 14% of the patients, further hair loss occurred, against 58% of the males who received a placebo.
In 48% of the males who received finasteride for a period of 12 months, the hair increased. The males who received a placebo only had an increase in 7%. The third study was done with 326 men (aged 20-41) with hair loss at the front and middle of the scalp. In 37% of these men, the treatment with finasteride resulted in an increase in hair growth, against 7% at placebo-basis. Finasteride was excellently endured in the clinical research.

The general endurance profile of finasteride was comparable to that of the placebo. The number of drop-outs as a result of side-effects was 1,7% for finasteride, and 2,1% for the placebo.
Most frequently reported side-effects were: less desire for sex: 1.8% on finasteride and 1.3% on placebo; difficulty in achieving an erection: 1.3 % on finasteride and 0.7 % on placebo; decrease in the amount of semen: 0.8 % on finasteride and 0.4 % on placebo. A large majority of the men who used finasteride (96%) did not report any side-effects of sexual nature. These side-effects went away in men who stopped taking PROPECIA. Moreover, the side-effects disappeared in many cases in which the patients preferred to continue with the therapy. The therapy with finasteride consisted of a daily intake of a pill of 1 mg. Finasteride has not yet been registered for the indication of baldness in the Netherlands. In the Netherlands, finasteride is only registered in a dose of 5 mg for the treatment of benign prostate enlargement. Data from several researches have been offered to the Medicines Evaluation Board (Dutch: College ter Beoordeling van Geneesmiddelen). After registration, Propecia will only be available at doctor's prescription. To date, Propecia has been registered amongst others in the United States, Mexico, New Zealand, Sweden, Finland, Denmark, Portugal and Italy.

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