Ultherapy™ Treatment Following Sculptra® Treatment

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

This clinical trial will evaluate clinical outcomes associated with the non-invasive Ultherapy™ treatment to improve skin laxity and tightening following a Sculptra® treatment.

Key facts

Study ID

NCT01422538

Run by

Ulthera, Inc

People needed

30

Starts

2011-05-01

Expected to finish

2012-09-01

Last updated by the study team

2017-12-13

Who can join

Age: 35 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female, aged 35 to 60 years.
• Subject in good health.
• Skin laxity in the lower face and neck.
• Grade 1 and 2 on the Knize Scale

You may not qualify if…

• 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.
• No scarring in areas to be treated.
• Any open facial wounds or lesions.
• Acne on the face.
• Patients who have a history with keloid formation or hypertropic scarring
• Patients who have a hypersensitivity to injectable poly-L-lactic acid
• Presence of a metal stent or implant in the facial area to be treated.

Where it is running

• EpiCentre Park Lane — Dallas, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.