Triactol Research  Clinical Test Results

Triactol Research Clinical Test Results

The emergence of Triactol™ Bust Serum is based on the result of several careful and systematic research studies

  • Numerous studies have demonstrated the safety and efficacy of Pueraria Mirifica.
  • Triactol is Dermatologically Tested- A total of 52 subjects completed the HRIPT (Human Repeat Insult Patch Test) study. No adverse reactions of any kind were reported during the course of this study.
  • No adverse reactions were recorded in 58 subjects who used Triactol™ Bust Serum in 2 in vivo clinical trials

Triactol Clinical Trial #1

Title: An open-label study was conducted to assess the efficacy & safety of Triactol™ Bust Serum among healthy female subjects.

  • All subjects were advised to apply Triactol™ Bust Serum twice daily
  • Results were taken via physical examination with interviews were gathered at day 0, day 21 (3 weeks) and day 42 (6 weeks)
  • At the final visit, questionnaires were administered to assess product safety and acceptance

1. Firming & Lifting Effects

triactol research firming and lifting
triactol research

Observations:

  • 75% of subjects experienced significant lifting and firming on day 21
  • Up to 94% of subjects experienced significant lifting and firming on day 42

2. Breast Enlargement Effect

Noticeable enlargement as early as 21 days of
application

At day 42,

  • 81% of the subjects experienced improvement in bust circumference
  • More than half (56%) of the subjects reported improvement to a cup size( 2cm) or more in 6 weeks

3. Product Acceptance & Others

Other important findings:

  • None of the subjects experienced any adverse reactions during this trial1
  • Reduction in wrinkle appearance & stretch marks on the bust area were reported
  • All of the subjects who tried other bust serums prefered Triactol™ Bust Serum1
  • 81% of the subjects experienced improved self confidence after using Triactol™ Bust Serum

Click HERE To Go To Triactol Product Page

Clinical Trial #2

Conducted by an independent 3rd party skin research centre (Data on File)
Objective: To evaluate the efficacy of Triactol™ on Bust Enlargement, Bust Firming and Bust Lifting

  • 42 subjects :Test group (20) and placebo group (22)
  • All subjects applied Triactol™ Bust Serum twice daily
  • Results were taken at the 3rd and 6th week
  • All data obtained were analysed using the paired t-test, ANCOVA and Chi-square test of the SPSS® 11.5 package programme

1.Breast Firming & Lifting

Significant improvements of bust angle and length observed in the test group after 3 weeks of bust serum application,
which was further enhanced after 6 weeks of bust serum application.

2.Breast Enlargement (Breast Volume)

triactol research breast volume
triactol research breast volume

Change of the bust volume was analysed by 3D Image Analysis GFM PRIMOS body® (GFMesstechnik GmbH, Germany) at baseline and at 3-week intervals during the 6-week treatment period

  • Significant improvements were observed in the subjects using Triactol™ after 3 weeks of application and this was further enhanced after 6 weeks.
  • Mean size attained after 6 weeks is +119.92cc
  • The maximum size attained was +339.41cc after 6 weeks (bigger than a small (240 cc for 2 breasts) saline breast implant

3. Breast Enlargement (circumference)

  • Significant breast circumference improvement was observed in the test group, after 6 weeks of bust serum application.
  • Maximum improvement in breast circumference is up to 2.4cm.
  • Mean (average) improvement is 0.58cm.
triactol research circumference
4.Breast Elasticity

Test group experienced significant breast elasticity improvement compared with that of placebo, after 3 & 6 weeks of bust serum application.

Conclusion

The results of the in vivo instrumental assessments and self assessment studies demonstrated bust enlargement, bust firming and bust lifting after applying Triactol™ Bust Serum for 3-6 weeks.

No adverse events were reported during the course of the study!

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