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The Treatment of Acne Vulgaris With Radiofrequency Device
This study has been withdrawn prior to recruitment.
Sponsored by: Alma Lasers
Information provided by: Alma Lasers
ClinicalTrials.gov Identifier: NCT00441805
  Purpose

Radiofrequency emmitting device, normaly used for thermage treatments will be used on 22 mild to moderate acne patients faces.

The aim of the study is to check whether RF heating of subcutaneous and dermis will improve acne in needed patients.


Condition Intervention
Acne Vulgaris
Device: Radio Frequency

MedlinePlus related topics: Acne
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Dose Comparison, Single Group Assignment, Safety/Efficacy Study
Official Title: The Treatment of Acne Vulgaris With Radiofrequency Device

Further study details as provided by Alma Lasers:

Estimated Enrollment: 22
Study Start Date: November 2006
Estimated Study Completion Date: September 2007
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • mild-moderate Acne
  • age over 18
  • otherwise healthy

Exclusion Criteria:

  • age under 18
  • pregnancy
  • systemic acne treatment in the last month
  • local acne treatment in the last month
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00441805

Locations
Israel
Lase Ohr clinic
Jerusalem, Israel
Sponsors and Collaborators
Alma Lasers
Investigators
Study Director: Yussi Levcelter, Dr. Alma Lasers LTD
  More Information

Study ID Numbers: AL-RF/ACN02/06IL CTIL
Study First Received: February 27, 2007
Last Updated: September 22, 2007
ClinicalTrials.gov Identifier: NCT00441805  
Health Authority: Israel: Ministry of Health

Keywords provided by Alma Lasers:
Acne
RadioFrequency

Study placed in the following topic categories:
Exanthema
Facial Dermatoses
Facies
Skin Diseases
Sebaceous Gland Diseases
Acne Vulgaris

Additional relevant MeSH terms:
Acneiform Eruptions

ClinicalTrials.gov processed this record on January 14, 2009