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

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Brief Title

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

Official Title

Evaluation of the Efficacy of the Cosmetic Lotion M.P.A.F. (Mixture of Paraffin, Alcohol and Fur) MEXIS PATENT in the Treatment of Androgenetic Alopecia by Decreasing of Hair Loss and Strengthening and Thickening of Hair in Males and Females.

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.
    


Study Type

Interventional


Primary Outcome

Change of the Amount of Hair Loss in a Pull Test

Secondary Outcome

 Change of Sebum on a Sebum-meter

Condition

Androgenetic Alopecia

Intervention

Hair loss prevention lotion

Study Arms / Comparison Groups

 Volunteers
Description:  20 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

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Other

Estimated Enrollment

20

Start Date

February 2001

Completion Date

June 2001

Primary Completion Date

June 2001

Eligibility Criteria

        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
      

Gender

All

Ages

18 Years - 70 Years

Accepts Healthy Volunteers

Accepts Healthy Volunteers

Contacts

Fulvio Marzatico, Monitor, , 

Location Countries

Greece

Location Countries

Greece

Administrative Informations


NCT ID

NCT01701271

Organization ID

MEXIS-HAIR LOSS-STUDY 1.2012


Responsible Party

Sponsor

Study Sponsor

Mexis George


Study Sponsor

Fulvio Marzatico, Monitor, Study Chair, Bio Basic EuropeResearch, Development and Dermo-Cosmetoligical Documentation


Verification Date

January 2016