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临床试验/IRCT20150101020514N24
IRCT20150101020514N24招募中2 期

Evaluating the safety and effectiveness of injectable gel with the Perjunse brand, for correcting nasolabial folds, before and after single clinical trial

Pars Fardad Nano Technology Company0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • 18-65 year old men and women
  • Moderate to severe nasolabial folds based on Allergan criteria
  • The opportunity to accompany the visit programs and study process.
  • Signing the informed consent form and agree to a 6-month follow-up

排除标准

  • Previous hyaluronic acid (HA)-based dermal filler treatment(s) injected within the last 12 months prior to enrollment.
  • Cosmetic facial procedures (chemical peel, laser, radio frequency, dermabrasion, ablative or non-ablative procedures), Botox) in the lower 2/3 of the face, within 3 months prior to study entry
  • Planning to undergo any of these procedures at any time during the study
  • Any cosmetic facial procedures during last 3 months
  • Allergy to gram positive bacteria protein, gel ingredients
  • Auto immune or immune deficiency diseases

研究者

发起方
Pars Fardad Nano Technology Company

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