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

Skin Laxity Clinical Trial

Official title:
Feasibility Study: Comparison Of Advil® Vs. Lortab® For Reducing Discomfort Associated With Ultherapy™ Treatment

Clinical Trial Summary

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

Clinical Trial Description

This trial is a prospective, single-site, double-blinded, randomized trial. All study subjects will receive a full face and neck Ultherapy treatment. Subjects will be randomized to receive one of two pain medications prior to treatment. Each subject will be asked to rate the level of discomfort during the Ultherapy treatment. All study subjects will be followed for 90 days following treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01708473
Study type Interventional
Source Merz Pharmaceuticals, LLC
Contact
Status Completed
Phase N/A
Start date July 2011
Completion date February 2012
View Details
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