Ice Versus EMLA for Pain in Laser Hair Removal
Running, not enrolling · Phase 4
Conditions studied: Hair Removal
In brief
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.
Key facts
- Study ID
- NCT02318654
- Run by
- Northwestern University
- People needed
- 30
- Starts
- 2014-12-30
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-07-01
Who can join
Age: 18 and older, up to 65. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Subjects are Caucasian or Asian females.
- Subjects are 18-65 years old.
- Subjects have Fitzpatrick skin type I-III and coarse dark axillary hair.
- Subjects are in good health.
- Subjects can provide informed consent.
- Subjects have the willingness and the ability to understand and communicate with the investigators.
You may not qualify if…
- Subjects who are allergic to lidocaine or prilocaine.
- History of methemoglobinemia.
- History of recurrent petechial or purpuric lesions.
- Bleeding tendency or coagulopathy.
- History of laser treatment in axilla.
- History of keloid or hypertrophic scarring.
- Pregnant or lactating or intends to become pregnant in the next 3 months.
- Active skin disease or skin infection in the treatment area.
- Subjects with known mental illness or other psychological conditions, such as psychotic disorders, mood disorders, anxiety disorders and cognitive disorders.
- History of cold urticaria.
- History of current injury or abnormal skin sensation.
- Unable to understand the protocol or to give informed consent.
- 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.
Where it is running
- Northwestern University Feinberg School of Medicine, Department of Dermatology — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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