跳至主要内容
临床试验/NL-OMON51645
NL-OMON51645撤回4 期

Post-market Clinical Investigation of High-Volume Anesthesia (Local Tumescent Anesthesia) used with the miraDry Treatment for Axillary Hyperhidrosis - miraDry Postmarket Tumescent Anesthesia Study

miraDry, Inc.0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
撤回
发起方
miraDry, Inc.
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Inclusion Criteria. Candidates for this study must meet ALL of the following
  • a) Adults (aged >=18 years) at time of consent.
  • b) A HDSS score of 3 or 4.
  • c) Excess sweating evidenced by at least two of the following:
  • a. Impairs daily activities
  • b. Frequency of at least one episode per week
  • c. Age of onset less than 25 years old
  • d. Positive family history
  • e. Cessation of focal sweating during sleep
  • d) In the opinion of the physician, treatment with the miraDry System is
  • technically feasible and clinically indicated.
  • e) Willing and able to comply with protocol requirements and all study visits.
  • f) Female patients of child-bearing potential must not be pregnant or lactating
  • and must agree to not become pregnant during the course of the study.

排除标准

  • Exclusion Criteria. Candidates will be excluded if ANY of the following
  • conditions apply:
  • a) A cardiac pacemaker or cardiac defibrillator or other electronic implant.
  • b) Requires supplemental oxygen.
  • c) Known resistance to or history of intolerance of local anesthesia including
  • lidocaine and epinephrine.
  • d) Secondary excess sweating due to medications, infections, malignancy.
  • e) Evidence of active infection.
  • f) Prior liposuction or other dissection surgery for axillary excess sweating.
  • g) Oral anticholinergic medication use (e.g., Glycopyrrolate) or cholinomimetic
  • medication use within the last 4 weeks or planned use during the study*s
  • follow-up phase.
  • h) Botulinum treatment of the axilla within the last 12 months.
  • i) Currently participating in or recently participated in another clinical
  • trial (within the last 30 days).
  • j) History of or current neurologic deficit in the treatment area and/or limb.
  • k) History of cancer with the exception of (1) successfully treated basal cell
  • or squamous cell carcinoma of the skin or (2) a history of successfully treated
  • cancer that have been disease-free for five years.

研究者

发起方
miraDry, Inc.

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