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临床试验/NCT01422538
NCT01422538已完成不适用

Evaluation of the Ulthera® System for Lifting and Tightening the Face and Neck Following Sculptra® Treatment

Ulthera, Inc1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2011年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Ulthera, Inc
入组人数
30
试验地点
1
主要终点
Lifting and Tightening of Skin as Determined by Masked Assessment of Pre- and Post-treatment Photographs.

研究概览

简要总结

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

详细描述

This study is a prospective,single-center, randomized clinical trial. Up to thirty (30) subjects will be treated. Enrolled subjects will be assigned to one of three (3) groups. Up to 10 subjects per group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
35 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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.

研究组 & 干预措施

Group A

Active Comparator

Subjects will receive Ulthera® System alone.

干预措施: Ulthera® System (Device)

Group B

Active Comparator

Sculptra® only

干预措施: Sculptra® (Drug)

Group C

Active Comparator

Sculptra® treatment followed by Ultherapy™ treatment

干预措施: Sculptra® treatment followed by Ultherapy™ treatment (Other)

结局指标

主要结局

Lifting and Tightening of Skin as Determined by Masked Assessment of Pre- and Post-treatment Photographs.

时间窗: 90 days post-treatment

Three masked assessors reviewed pre- and 90 days post-treatment photos from 29 subjects who returned for their 90-day follow-up visit, assessing for improvement in skin laxity at 90 days post-treatment compared to baseline, i.e., lifted and tightened skin in the areas treated with the assigned study treatment based on the assigned study arm.

次要结局

  • Overall Aesthetic Improvement at 180 Days Post-treatment(180 days post-treatment)
  • Subject Satisfaction at 180 Days Post-treatment(180 days post-treatment)
  • Overall Aesthetic Improvement at 90 Days Post-treatment(90 days post-treatment.)
  • Subject Satisfaction at 90 Days Post-treatment(90 days post-treatment.)

研究者

发起方
Ulthera, Inc
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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