Presto Gel - Hemorrhoids
Treatment
The Research and Development of Presto Gel a Natural
Hemorrhoids Treatment
The Research
Methods:
Clinical trial – Phase
I
Phase period: Two months, from the beginning of May 2006
through the end of June 2006, with the participation of 95
patients using the four preparations of the formulas named A,
B, C, and D for trial purposes (two week trial period for each
formula).
All four formulas contain the same ingredients, but each
formula differs in its composition from the others in the ratio
of its quantitative relation between the ingredients.
All participants were divided by the ISB method (Illness
Stage Breakdown) into four main groups according to the
severity of each one’s condition. Details of each participant
were registered: age, general health condition, eating habits,
type of employment, level of activity at work, addictions (if
such exist), hobbies during leisure hours and medical treatment
concerning those taking prescription medicines (temporarily
and/or regularly). Each participant from each group got one
formula out of the four for an experimental application of two
weeks, along with clear instructions for use, dosage, etc,
according to the severity of his/her condition.
After two weeks, reactions and results of each participant
from each group were examined. The data were registered in the
personal file of each participant.
During the next two weeks each participant from each group
got another formula for experimental application. In this way,
the experiments went on every two weeks until each participant
from each group had tried each of the four formulas,
rotationally.
The reactions and results were consistently registered every
two weeks at the end of every experiment with each formula.
At the end of the first phase of the trial, an in-depth and
comprehensive examination was carried out.
After reaching conclusions, the aim was to improve the
interaction between ingredients, hence the ingredients of all
four formulas were mixed and re-combined to create two new
formulas. The ingredients in each formula and the quantitative
ratio between the ingredients were essentially different
from each other.
Clinical trial – Phase
II
Phase period: Four weeks, from the end of August 2006 till
the end of September 2006.
72 patients participated in this phase, using the two new
formulas named E and F for trial purposes.
The ways and methods of trial in this phase are similar to
those used in the first phase, with two weeks allotted for each
of the two formulas. All participants reported good
results.
At the end of this phase a thorough examination was carried
out. Each and every detail concerning the reactions of each
participant resulting from use of the two formulas was studied
meticulously. Based on the examination’s conclusions and after
additional study of professional and research literature and
further consultations with professionals in the field of
scientific research, the ingredients of the two formulas, E and
F, were mixed with a reformed quantitative relation between
them and then put together in one formula, in order to
optimally enhance, widen and improve the therapeutic activity
and effectiveness of the preparation.
Clinical trial – Phase III
Phase period: Six months, from the end of October 2006 till
the end of April 2007. In this phase 61 patients participated,
using the one formula named P for trial purposes.
The results of this experiment were phenomenal, and beyond
all expectations. All 61 participants reported an immediate,
significant and prolonged relief in the pain and pressure upon
application of the preparation.
With continued use of the preparation many people reported a
substantial wide spectrum improvement in their general
condition.
Due to the outstanding results the preparation produces
quickly and effectively, we chose the most befitting name for
it – Presto Gel; The word “Presto” originally from the Latin
and later the Italian, meaning “Rapid, Quick, Miraculous”.
Hemorrhoids Treatment - Clinical
Trials Results
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