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临床试验/NCT06336759
NCT06336759已完成不适用

Prospective Clinical Trial Evaluating the Safety and Efficacy of Restylane Lyft and Defyne for Contouring the Jawline

Erevna Innovations Inc.2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年11月11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
40
试验地点
2
主要终点
Frequency of subjects displaying at least a one grade improvement since Baseline, on the Raspaldo (2008) Jawline Scale

研究概览

简要总结

The study's goal is to assess the safety and efficacy of two hyaluronic acid products, Restylane Lyft and Defyne, for contouring the jawline and chin, in order to address concerns regarding contour deficiencies among patients seeking aesthetic treatments.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • A score > 1 on the Raspaldo Jawline Scale, as assessed by the treating physician at Baseline. A possible secondary deficit of the chin is allowed.
  • Males and females aged > 18 years.
  • Ability to adequately understand the verbal explanations and the written subject information provided in local language and ability and willingness to give consent to participate in the study.
  • Signed and dated informed consent to participate in the study.
  • If female of childbearing potential: a negative urine pregnancy test before all treatments is required.

排除标准

  • Current pregnancy or lactation [sexually active women of childbearing age must agree to use medically acceptable methods of contraception for the duration of this study (e.g., oral contraceptives, condoms, intrauterine device, shot/injection, patch)].
  • Subjects presenting with known allergy to hyaluronic acid fillers or amide local anesthetics.
  • Subjects presenting with porphyria.
  • Subjects with active disease, such as inflammation, infection or tumors, in or near the intended treatment sites.
  • Subjects with history of bleeding disorders or subjects taking thrombolytics or anticoagulants.
  • Subjects taking inhibitors of platelet aggregation (e.g., Aspirin or other non-steroid anti-inflammatory drugs [NSAIDs]), within 2 weeks before treatment.
  • Subjects using immunosuppressants.
  • History of permanent implants in the lower face.
  • History of other treatment/procedure that, in the treating investigator's opinion, would interfere with the study injections and/or study assessments or exposes the subject to undue risk by study participation.
  • Visible markings that in the treating investigator's opinion, may interfere with results or assessments.
  • Inability to comply with follow-up and abstain from other treatments in the region of interest during the study period.
  • Heavy smokers, classified as smoking more than 12 cigarettes per day.
  • History of severe or multiple allergies manifested by anaphylaxis.
  • Previous tissue revitalization therapy in the treatment area within 6 months before treatment with laser or light, mesotherapy, radiofrequency, ultrasound, cryotherapy, chemical peeling, or dermabrasion.
  • Previous treatment with neurotoxins in the area under assessment, within 6 months prior to enrolment.
  • Previous treatment with soft tissue fillers in the area under assessment, within 12 months prior to enrolment.
  • Cancer or precancer in the treatment area (e.g., actinic keratosis).
  • Subjects with a tendency to form hypertrophic scars or any other healing disorders.
  • Subjects with a mean skin thickness in the treatment areas between 1.29mm and 1.49mm (ie, "normal" thickness), as determined by ultrasound at Baseline, to ensure no overlap between the two strata (ie, thin and thick skin).

结局指标

主要结局

Frequency of subjects displaying at least a one grade improvement since Baseline, on the Raspaldo (2008) Jawline Scale

时间窗: Baseline to Month 3

The Jawline (Raspaldo 2008) Scale is a 5 point Likert scale ranging from "severe depression or atrophy" (grade 4) to "normal" (grade 1) used by the blinded evaluator to assess the jawline

Frequency of subjects having at least "improved" since Baseline, as per the Global Aesthetic Improvement Scale (GAIS)

时间窗: Baseline to Month 3

The Global Aesthetic Improvement Scale is a graded Likert scale with assessments ranging form "very much worse" (grade -3) to "very much improved" (grade 3).

次要结局

  • Frequency of subjects displaying at least a one grade improvement since Baseline, on the Raspaldo Jawline Scale(Baseline to Month 6)
  • Frequency of subjects having at least "improved" since Baseline, as per the Global Aesthetic Improvement Scale (GAIS)(Baseline to Month 6)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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