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临床试验/NCT03320824
NCT03320824已完成不适用

A Randomized, Controlled, Evaluator-Blinded, Multi-Center Study to Evaluate the Effectiveness and Safety of Restylane Kysse Versus a Control in the Augmentation of Soft Tissue Fullness of the Lip

Galderma R&D28 个研究点 分布在 1 个国家目标入组 273 人开始时间: 2017年11月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Galderma R&D
入组人数
273
试验地点
28
主要终点
Assess Effectiveness of the Treatment Using the Medicis Lip Fullness Scale (MLFS)

研究概览

简要总结

To demonstrate non-inferiority of Kysse versus a control in lip fullness augmentation

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Subjects willing to comply with the requirements of the study and providing a signed written informed consent.
  • Males or non-pregnant, non-breastfeeding females, 22 years of age or older.
  • Seeking augmentation therapy for the lips

排除标准

  • Allergy of hypersensitivity to any injectable hyaluronic acid gel or to gram positive bacterial proteins.
  • Allergy or hypersensitivity to lidocaine or other amide-type anesthetics, or topical anesthetics or nerve blocking agents.

结局指标

主要结局

Assess Effectiveness of the Treatment Using the Medicis Lip Fullness Scale (MLFS)

时间窗: 8 weeks after last injection

The MLFS is a validated photograph-based outcome instrument that is designed specifically for quantifying lip fullness. Scoring of lip fullness (grades 0-5, with a higher score reflecting greater lip fullness) was based on visual live assessment by the Blinded Evaluator at defined time points, and not on a comparison to the baseline appearance. Effectiveness is defined as change from baseline at 8 weeks after last injection of New Dermal Filler or Dermal Filler (control).

次要结局

  • Assess Effectiveness of the New Dermal Filler Treatment in the Upper & Lower Lips Using the Medicis Lip Fullness Scale(16, 24, 32, 40, and 48 weeks)
  • Assess Aesthetic Improvement in the Perioral Rhytids & Oral Commissures After New Dermal Filler Treatment Using the Wrinkle Assessment Scale (Change From Baseline, Blinded Evaluator)(8, 16, 24, 32, 40, and 48 weeks after last injection)
  • Assess Overall Aesthetic Improvement After New Dermal Filler Treatment Using the Global Aesthetic Improvement Scale Determined by Response Rates, Subject Assessment(8, 16, 24, 32, 40, and 48 weeks)
  • Assess Subject Satisfaction With New Dermal Filler Treatment Using the FACE-Q(8, 16, 24, 32, 40, and 48 weeks)
  • Assess Aesthetic Improvement in the Perioral Rhytids & Oral Commissures After New Dermal Filler Treatment Using the Wrinkle Assessment Scale (Response Rates, Blinded Evaluator)(8, 16, 24, 32, 40, and 48 weeks)
  • Assess Overall Aesthetic Improvement After New Dermal Filler Treatment Using the Global Aesthetic Improvement Scale, Treating Investigator(8, 16, 24, 32, 40, and 48 weeks)
  • Assessment of Improvement in Lip Fullness After New Dermal Filler Treatment, by Independent Photographic Reviewer(8, 24, 40, and 48 weeks)

研究者

发起方
Galderma R&D
申办方类型
Industry
责任方
Sponsor

研究点 (28)

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