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临床试验/NCT07588243
NCT07588243进行中(未招募)不适用

A Pivotal Clinical Study to Evaluate the Efficacy and Safety of Ultra in Promoting Hair Regrowth

CynosureLutronic4 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2026年2月19日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
44
试验地点
4

研究概览

简要总结

The goal of this clinical study is to evaluate the efficacy and safety of the Ultra device for the treatment of hair regrowth by assessing the improvement of hair density and hair shaft diameter.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 22 - 70 years old
  • Is willing to undergo study device use.
  • Fitzpatrick skin type I-VI
  • Clinical diagnosis of androgenetic alopecia (Norwood-Hamilton II-V or Ludwig I-II)
  • Willing to avoid significant changes to hair (such as drastic haircuts and dying hair) during their involvement in the study.
  • Willing to maintain current diet and exercise routine throughout study duration.
  • Understands and accepts the study condition to not receive any other procedures to the treatment area or to undergo any procedures, take any medications, supplements, or partake in any other treatments indicated for hair growth throughout the length of the study.
  • Understands and accepts the study condition of and agrees that he or she is able to be present for all study visits.
  • Willing to comply with all requirements of the study and is able to provide written informed consent.

排除标准

  • Is female and pregnant, has been pregnant within the last 3 months, is currently breast feeding, or planning a pregnancy during the study period.
  • Has a diagnosis of other forms of alopecia (e.g., scarring alopecia, alopecia areata)
  • Has recent use (within 6 months) of a systemic hair growth medications (e.g., oral finasteride).
  • Inconsistent use of vitamins that can affect hair growth - must have stabilized use for at least 6 months prior to first treatment.
  • Had previous treatment (such as laser or topical) to scalp within 6 months.
  • Has a malignant disease, cancer, or uncontrolled medical condition.
  • Has an impaired immune system due to immunosuppressive diseases, such as AIDS and HIV, or use of immunosuppressive medications

研究组 & 干预措施

Ultra Treatment

Experimental

干预措施: Low Level Laser Therapy (Device)

研究者

发起方
CynosureLutronic
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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