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临床试验/NCT03194269
NCT03194269已完成4 期

FOLD: Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Prominent Ears

Allergan12 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2017年8月17日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
Allergan
入组人数
84
试验地点
12
主要终点
Change from baseline pre-insertion in EAR-Q Ears Appearance Questionnaire score

研究概览

简要总结

This is an open-label, prospective, uncontrolled, single arm, post-marketing study of the long-term safety and performance of EARFOLD® Implantable Clip System.

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

入选标准

  • Subjects who have ear prominence and/or have significant asymmetry

排除标准

  • Subjects planning to use EARFOLD® in conjunction with other procedures (e.g. cartilage scoring, conchal reduction or concho-mastoid sutures) for correction of prominent ears are excluded
  • Patients with impaired healing (e.g., current smokers, diabetic patients, patients with autoimmune disorders such as Ehlers-Danlos Syndrome or Scleroderma)
  • Patients with an active infection, local or systemic
  • Patients with known nickel or gold allergies.

结局指标

主要结局

Change from baseline pre-insertion in EAR-Q Ears Appearance Questionnaire score

时间窗: Baseline to month 3

EAR-Q Ears Appearance Questionnaire is on a 4 point scale (1=Not at all, 2=A little bit, 3=Quite a bit, 4=Very much)

次要结局

  • Change from baseline pre-insertion in EAR-Q Ears Appearance overall score at 24 months post-implantation(Baseline to Month 24)
  • Change from baseline of Short Form-10 score at Month 24 for subjects under 18 years old(Baseline to Month 24)
  • Change in maximum helix to scalp distance from PREFOLD® insertion to post insertion distances at Month 12(Baseline to Month 12)
  • Change from baseline pre-insertion in EAR-Q School Function Questionnaire at Month 3(Baseline to Month 3)
  • Change from baseline pre-insertion in EAR-Q Ears Appearance overall score at 12 months post-implantation(Baseline to Month 12)
  • Percentage of patients that require re-operation at any moment(24 months)
  • Change from baseline of Short Form-12 score at Month 24 for subjects over 18 years(Baseline to Month 24)
  • Change from baseline of Short Form-12 score at Month 12 for subjects over 18 years(Baseline to Month 12)
  • Change from baseline of Short Form-10 score at Month 3 for subjects under 18 years old(Baseline to Month 3)
  • Change from baseline of Short Form-10 score at Month 12 for subjects under 18 years old(Baseline to Month 12)
  • Percentage of patients with recurrence of ear prominence(24 months)
  • Change from baseline of Short Form-12 score at Month 3 for subjects over 18 years(Baseline to Month 3)
  • Change from baseline in maximum helix to scalp distance from before PREFOLD® insertion at Month 12(Baseline to Month 12)
  • Change from baseline pre-insertion in EAR-Q Psychological Function Questionnaire at Month 3(Baseline to Month 3)
  • Change from baseline in maximum helix to scalp distance from before PREFOLD® insertion at Month 3(Baseline to Month 3)
  • Change from baseline in maximum helix to scalp distance from before PREFOLD® insertion at Month 24(Baseline to Month 24)
  • Maintenance of maximum helix to scalp distance at 12 months compared to 3 months visit post insertion of EARFOLD(Month 3 to Month 12)
  • Maintenance of maximum helix to scalp distance at 24 months compared to 3 months visit post insertion of EARFOLD(Month 3 to Month 24)
  • Change in maximum helix to scalp distance from PREFOLD® insertion to post insertion distances at Month 3(Baseline to Month 3)
  • Change in maximum helix to scalp distance from PREFOLD® insertion to post insertion distances at Month 24(Baseline to Month 24)
  • Duration of EARFOLD® insertion procedure(Duration of surgery)
  • Change from baseline pre-insertion in EAR-Q Social Function Questionnaire at Month 3(Baseline to Month 3)
  • Change from baseline pre-insertion in EAR-Q Social Function Questionnaire at Month 12(Baseline to Month 12)
  • Change from baseline pre-insertion in EAR-Q Social Function Questionnaire at Month 24(Baseline to Month 24)
  • Change from baseline pre-insertion in EAR-Q School Function Questionnaire at Month 12(Baseline to Month 12)
  • Change from baseline pre-insertion in EAR-Q Psychological Function Questionnaire at Month 24(Baseline to Month 24)
  • Return to normal activities questionnaire after EARFOLD® surgery at Month 3(Month 3)
  • Change from baseline pre-insertion in EAR-Q School Function Questionnaire at Month 24(Baseline to Month 24)
  • Change from baseline pre-insertion in EAR-Q Psychological Function Questionnaire at Month 12(Baseline to Month 12)

研究者

发起方
Allergan
申办方类型
Industry
责任方
Sponsor

研究点 (12)

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