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临床试验/NCT03273543
NCT03273543已完成不适用

Premaxillary Injection for Perioral Rejuvenation and Upper Lip Enhancement

DeNova Research2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2017年11月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Upper Lip Projection

研究概览

简要总结

To determine if subjects who receive premaxillary injection demonstrate an increase in nasal tip projection and an associated increase in upper lip projection, and vermillion height.

研究设计

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

入排标准

年龄范围
21 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects Age 21 to
  • Subjects who demonstrate signs of perioral aging or poor upper lip projection.

排除标准

  • Subjects who plan to undergo peri oral neurotoxin treatments or ablative skin treatments, or have had either of these treatments in the previous 6 months, other injectable filler treatments during the course of the study.
  • Subjects who are pregnant or nursing.
  • Subjects with a known allergy or sensitivity to any component of the study ingredients.
  • Any history of rhinoplasty or nasal filler injections.
  • Recent history of upper lip augmentation (surgical and non-surgical) within the last 12 months.
  • Any history of lip lift or other surgical procedures involving the upper lip.
  • Any history of chin augmentation (surgical and non-surgical).
  • Any history of orthognathic surgery.
  • Any history of bleeding disorders (iatrogenic or otherwise).
  • Current history of chronic drug or alcohol abuse.
  • Concurrent therapy that, in the investigator's opinion, would interfere with the evaluation of the safety or efficacy of the study product (i.e. immunosuppressive therapy).
  • Subjects who, in the Investigator's opinion, have a history of poor cooperation, non¬compliance with medical treatment or unreliability.

结局指标

主要结局

Upper Lip Projection

时间窗: Baseline and 2 months

baseline upper lip position will recorded by measuring the Z-angle, which is the intersection of the Frankfort horizontal line and the profile line as described by Merrifield. From the straight portrait image, the ratio of the upper lip vermillion height to the lower lip vermillion height will be documented. Upper lip projection was assessed via measurement of the Z angle. On each subject's right lateral view photograph, a profile line was drawn tangential to the pogonion of the chin and to the most anterior point of the upper lip. A second line was drawn along the Frankfort horizontal plane. The resulting angle at which these two lines intersected corresponded to the Z angle. A decrease in the Z angle to a more acute value on post-treatment photographs would correspond to an increase in upper lip projection.

Nasal Tip Projection

时间窗: Baseline and 2 months

Baseline nasal projection measurements will be documented according to Goode's ratio. The Goode ratio was used as a measurement of tip projection and is defined as the ratio of the nasal height in relation to the nasal length. For each subject's right lateral view photograph, the nasal height was measured as the length of a line drawn from the alar-facial groove to the tip-defining point, and the nasal length was measured as the length of the line drawn from the nasion to the tip-defining point. The nasal height value was then divided by the nasal length value to determine the Goode ratio for a given photograph. The ratio of the line from the alar crease to the nasal tip to the nasion to the nasal tip should be . 55. If it is more than that the nose is overprojected, if it is under that ratio the nose is underprojected.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Steven H. Dayan

MD, FACS

DeNova Research

研究点 (2)

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