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临床试验/NCT04112017
NCT04112017终止不适用

A Multicenter, Randomized, No-treatment Controlled, Parallel, Evaluator-blind, Medical Device Pivotal Study to Evaluate the Effectiveness and Safety of YVOIRE Y-Solution 360 Injected Into Dorsal Hand for Hand Augmentation to Correct Volume Loss

LG Chem2 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2019年9月27日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
116
试验地点
2
主要终点
≥ 1 grade improvement on Hand Volume Rating Scale (HVRS) as assessed by the evaluator-blinded

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness and safety of YVOIRE Y-Solution 360 in the treatment of dorsal hand to correct volume loss.

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
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 19 Years and older
  • Hand Volume Rating Scale (HVRS) of grade 2 or 3 with both hands
  • Participants who are willing to undergo the treatment of dorsal hand to correct volume loss

排除标准

  • Congenital defect, external injuries, lipodystrophy, unhealed wound, disease related-abnormalities, or tumors on the dorsal hands
  • Active inflammation or infection on the dorsal hands
  • Received anti-coagulation therapy, anti-platelet therapy, or expected to require repeated treatment within 2 weeks prior to visit 2 (randomization)
  • Had locally applied ointments (steroid, retinoid, anti-wrinkle production, tanning, or any other form of irritating product) or expected to require repeated treatment within 4 weeks prior to visit 2 (randomization)
  • Received immuno-suppressive medication including systemic glucocorticoids or expected to require repeated treatment within 8 weeks prior to visit 2 (randomization)
  • Received NSAIDs, Vitamin E, or expected to require repeated treatment within 1 week prior to visit 2 (randomization)
  • Had dermal filler injections (HA, CaHA, silicon, PAAG, PMMA etc.), Botulinum toxin therapy, adipose tissue transplantation, or esthetic surgery within 12 months prior to visit 2 (randomization)

结局指标

主要结局

≥ 1 grade improvement on Hand Volume Rating Scale (HVRS) as assessed by the evaluator-blinded

时间窗: 12 weeks after treatment

5-grade photonumeric hand grading scale (grade 0 - grade 4)

次要结局

  • ≥ 1 grade improvement on Hand Volume Rating Scale (HVRS) as assessed by the evaluator-blinded and the treating investigator(Up to 52 weeks after treatment)
  • ≥ 1 grade improvement on Global Aesthetic Improvement Scale (GAIS) as assessed by the treating investigator and the subject(Up to 52 weeks after treatment)
  • Change from baseline on Hand Volume Rating Scale (HVRS) as assessed by the evaluator-blinded and the treating investigator(Up to 52 weeks after treatment)
  • Change from baseline on Global Aesthetic Improvement Scale (GAIS) as assessed by the treating investigator and the subject(Up to 52 weeks after treatment)
  • Safety profile as assessed by incidence of adverse events(Up to 52 weeks after treatment)

研究者

发起方
LG Chem
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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