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Efficacy Study of a Cosmetic Lotion in the Treatment of Androgenetic Alopecia in Males and Females

Not Applicable
Completed
Conditions
Androgenetic Alopecia
Interventions
Other: Hair loss prevention lotion
Registration Number
NCT01701271
Lead Sponsor
Mexis George
Brief Summary

The purpose of this study is to determine whether the Hair Loss Prevention Lotion named MEXIS, M.P.A.F., M6S PATENT is effective in the treatment of Androgenetic Alopecia.

Detailed Description

This study verifies whether the tested product has any efficacy in the treatment of Androgenetic Alopecia.

* The evaluated product (Hair Loss prevention Lotion) is called:MEXIS, MPAF, M6S PATENT.

* 20 volunteers both men and women suffering from hair loss both in parties and over the entire scalp with age between 18 and 70 years have been selected for this test .

* Samples of the product have been applied following their usual use: as they are.

* On the selecting volunteers have been used:

1. The pull test by pulling with fingers of some hair and counting them to estimate the evolution of the pathology.

2. A sebum-meter to check the presence of scales on the scalp.

3. A polarized light video-camera to check the redness of the scalp and to have a picture of hair and scalp.

* Volunteers were also asked about:

* Fluffiness

* Sheen

* Itching

* Presence of scales on scalp

* Oily hair

* Product's acceptability

* The readings are taken at 0 time (basal value), after 15 days (t15), 30 days (t30), 45 days (t45), 45 days (t45), 60 days (t60) and 90 days (t90) by the experimenter in the medical studio. Then they analyzed and reported in a graph.

* Summarizing tables and graphs of the data were taken during experimentation.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Good state of general health
  • Suffering from hair loss
  • No pharmacological treatment in progress
  • Promise not to change the usual daily routine
  • No atopy in the anamnesis
Exclusion Criteria
  • Illness
  • Good state of hair
  • Pharmacological treatment in progress
  • Denial of the continuance of the usual daily routine
  • Atopy in the anamnesis

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
VolunteersHair loss prevention lotion20 volunteers both men and women with an age between 18 and 70 years suffering from Androgenetic Allopecia in several types apply on the scalp drops of the hair loss prevention lotion
Primary Outcome Measures
NameTimeMethod
Change of the Amount of Hair Loss in a Pull Testbaseline and 90 days

Measurement of the decrease of hair loss by pull test and pulling some hair with the fingers.

Measurements estimated and reported every 15 days. The Measure reports decrease in fallen hair

Change of the Density of the Hair on a Polarized Light Video-camera as a Measure of Efficacy.baseline and 90 days

Number of hair was assessed for each participant with a polarized light video-camera every 15 days for a total of 6 assessments

Secondary Outcome Measures
NameTimeMethod
Change of Sebum on a Sebum-meterbaseline and 90 days

Measurements checked and reported every 15 days of the decrease of existing sebum on the scalp of the volunteers with a sebum-meter.

Trial Locations

Locations (1)

George Mexis

🇬🇷

Athens, Greece

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