Expired Study
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Chicago, Illinois 60611


Purpose:

The primary objective of this study is to compare the efficacy of ice pack to topical eutectic mixture of local anesthesia (EMLA) for pain control in diode 810 nm laser axillary hair removal. This study is a pilot study designed to determine feasibility of these procedures.


Criteria:

Inclusion Criteria 1. Subjects are Caucasian or Asian females. 2. Subjects are 18-65 years old. 3. Subjects have Fitzpatrick skin type I-III and coarse dark axillary hair. 4. Subjects are in good health. 5. Subjects can provide informed consent. 6. Subjects have the willingness and the ability to understand and communicate with the investigators. Exclusion Criteria 1. Subjects who are allergic to lidocaine or prilocaine. 2. History of methemoglobinemia. 3. History of recurrent petechial or purpuric lesions. 4. Bleeding tendency or coagulopathy. 5. History of laser treatment in axilla. 6. History of keloid or hypertrophic scarring. 7. Pregnant or lactating or intends to become pregnant in the next 3 months. 8. Active skin disease or skin infection in the treatment area. 9. Subjects with known mental illness or other psychological conditions, such as psychotic disorders, mood disorders, anxiety disorders and cognitive disorders. 10. History of cold urticaria. 11. History of current injury or abnormal skin sensation. 12. Unable to understand the protocol or to give informed consent. 13. Any other condition that would, in the professional opinion of the investigator, potentially affect response or participation in the clinical clinical study, or would pose as an unacceptable risk to subject.


NCT ID:

NCT02318654


Primary Contact:

Principal Investigator
Murad Alam, MD
Northwestern University


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60611
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 23, 2017

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