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临床试验/NCT04279236
NCT04279236已完成不适用

A Prospective Multi-Center Study on the Performance of the Ponto Implant System Using Minimally Invasive Ponto Surgery (MIPS)

Oticon Medical8 个研究点 分布在 3 个国家目标入组 64 人开始时间: 2020年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
64
试验地点
8
主要终点
Implant/abutment complex capability to provide reliable anchorage for sound processor

研究概览

简要总结

This prospective, multi-center study funded by Oticon Medical AB will be conducted at six clinical sites in North America. Patients with a hearing loss and that are already planned for treatment with a percutaneous (through the skin) bone-anchored hearing system (BAHS) will be included in the study. The total number of participants included in the study will be 64.

The purpose of this study is to investigate the rate of successful BAHS use after implantation of the Ponto Implant system using the surgical technique Minimally Invasive Ponto Surgery (MIPS).

详细描述

This prospective, multi-centre study funded by Oticon Medical AB will be conducted at six clinical sites in North America. Patients with a hearing loss and that are already planned for treatment with a percutaneous (through the skin) bone-anchored hearing system (BAHS) will be included in the study. The total number of participants included in the study will be 64. Patients who are withdrawn from the study prior to completion will not be replaced.

The purpose of this study is to investigate the rate of successful BAHS use after implantation of the Ponto Implant system using the surgical technique Minimally Invasive Ponto Surgery (MIPS). The implant, coupled to a skin-penetrating abutment, is implanted in the bone behind the ear and is later loaded with a sound processor which transforms sound waves to sound vibrations that can be sent directly to the inner ear via the skull bone. The primary objective of this study is to investigate the proportion of implant/abutment complexes providing a reliable anchorage for a sound processor, 3 months after implantation/surgery.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • 18 years of age or older
  • Patient indicated for surgical intervention with a bone anchored hearing system according to local clinic's standard guidelines.
  • Normal bone quality and bone thickness above 3 mm, where no complications during surgery are expected.
  • Skin thickness of 12mm or less at the implant site

排除标准

  • Patients undergoing re-implantation
  • Patients who are unable or unwilling to follow investigational procedures/requirements, e.g. to complete quality of life scales.
  • Diseases or treatments known to compromise the bone quality at the implant site, e.g. radiotherapy, osteoporosis, diabetes mellitus
  • Known conditions (e.g. uncontrolled diabetes) that could jeopardize skin condition and wound healing over time as judged by the investigator.
  • Any other known condition that the investigator determines could interfere with compliance or study assessments.

结局指标

主要结局

Implant/abutment complex capability to provide reliable anchorage for sound processor

时间窗: 3 months after implant surgery (MIPS)

The variables assessed to determine reliable anchorage in the study are implant survival and stability, skin reactions, skin over-growth and pain preventing use of the sound processor. For a positive outcome of the primary endpoint (reliable anchorage), the implant should be in place and stable. without any adverse skin reactions or skin over-growth and pain preventing usage of the sound processor.

次要结局

  • IPS scores(12 months after implant surgery (MIPS))
  • Patient-perceived magnitude of pain around implant/abutment(12 months after implant surgery (MIPS))
  • Subjective benefit after MIPS surgery(12 months after implant surgery (MIPS))
  • Implant/abutment complex capability to provide reliable anchorage for sound processor(12 months after implant surgery (MIPS))
  • Wound dehiscence(12 months after implant surgery (MIPS))
  • Wound healing time(12 months after implant surgery (MIPS))
  • Implant survival(12 months after implant surgery (MIPS))
  • Implant stability(12 months after implant surgery (MIPS))
  • Holgers score ratings(12 months after implant surgery (MIPS))
  • Duration of surgery(At implant surgery (MIPS))
  • Patient-perceived presence of pain around implant/abutment(12 months after implant surgery (MIPS))
  • Patient-perceived presence of numbness around implant/abutment(12 months after implant surgery (MIPS))
  • Patient-perceived magnitude of numbness around implant/abutment(12 months after implant surgery (MIPS))
  • Skin/soft tissue overgrowth(12 months after implant surgery (MIPS))
  • Implant/abutment usage(12 months after implant surgery (MIPS))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (8)

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