Status:

COMPLETED

Safety and Efficacy of Using LEORTEC-300 System For Hair Removal Treatment

Lead Sponsor:

Leortec Medical Systems Ltd

Conditions:

Epilation

Eligibility:

All Genders

18-70 years

Phase:

PHASE1

PHASE2

Brief Summary

Removal of unwanted hair is one of the most commonly sought cosmetic solutions. Traditional methods, such as shaving, depilatories, tweezing and waxing result in only temporary hair removal, and thus ...

Detailed Description

STUDY OBJECTIVES 1. Primary Objective * Safety * To evaluate the safety of using LEORTEC-300 System for hair removal treatment, in different skin/hair colors and anatomical sites. 2. Second...

Eligibility Criteria

Inclusion

  • Healthy males/females between the ages of 18 to 70
  • Subject is willing to go trough hair removal treatment.
  • Subject understands the study procedure.
  • Subject is willing to sign the inform consent.
  • Subject must have the ability to comply with the study procedures and follow- up.

Exclusion

  • Age \< 18 years or \> 70 years.
  • Use of medication for which 400nm to 1400nm light exposure is contraindicated
  • Coagulation disorder.
  • Infection / abscess / pains in treatment target area.
  • Recently tanned skin.
  • Photosensitivity or allergy.
  • Psoriasis.
  • Skin cancer.
  • Diabetes.
  • Pregnancy.
  • Tattoo on targeted area.
  • History of keloid scarring.
  • Use of aspirin or antioxidants
  • Eczema or dermatitis.
  • Subject is suffering extreme general weakness.
  • Subject objects to the study protocol.
  • Physician objection.
  • Known cognitive or psychiatric disorder
  • Participation in any other clinical trial

Key Trial Info

Start Date :

July 1 2006

Trial Type :

INTERVENTIONAL

End Date :

September 1 2006

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT00348257

Start Date

July 1 2006

End Date

September 1 2006

Last Update

February 28 2007

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Elisha Hospital

Haifa, Israel, 34636