Feasibility Study: Compare the Effectiveness Between Two Pain Medications When Used Prior to Ultherapy™ Treatments

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

This study will compare the effectiveness of two pain medications for reducing discomfort during an Ultherapy treatment.

Key facts

Study ID

NCT01708473

Run by

Ulthera, Inc

People needed

20

Starts

2011-07-01

Expected to finish

2012-02-01

Last updated by the study team

2017-11-24

Who can join

Age: 30 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female, aged 30 to 65 years
• Subject in good health
• Skin laxity on the upper and lower face and neck
• Understands and accepts the obligation not to undergo any other procedures in the areas to be treated through the followup period

You may not qualify if…

• Known sensitivity to ibuprofen, acetaminophen, or opiates
• Presence of an active systemic or local skin disease that may affect wound healing
• Severe solar elastosis
• Excessive subcutaneous fat in the face and neck
• Excessive skin laxity on the face and neck
• Significant scarring in areas to be treated
• Significant open facial wounds or lesions
• Severe or cystic acne on the face
• Presence of a metal stent or implant in the facial area to be treated

Where it is running

• Dermatology, Cosmetic & Laser Surgery — Rockville, Maryland, United States

Full record on ClinicalTrials.gov

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