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临床试验/NCT00762944
NCT00762944已完成不适用

Survivibility of the Total Temporomandibular Joint Replacement System

Zimmer Biomet4 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2005年9月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Zimmer Biomet
入组人数
93
试验地点
4
主要终点
Time to Revision

研究概览

简要总结

Post-Approval Study (PMA CoA) in Order to Obtain Additional Long Term Safety and Effectiveness Data [PMA P020016]

详细描述

An additional three-year follow-up data will be collected on subjects previously enrolled in the PMA study, who had not completed follow-up prior to the PMA approval [PMA P020016].

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

  • Patients requiring total joint reconstruction due to:
  • Arthritis (osteoarthritis, rheumatoid, traumatic) malignancy Ankylosis functional deformity Avascular necrosis revisions Benign neoplasms fracture Multiple operated joints
  • Patients who are skeletally mature.
  • Patients must have at least one of the following criteria for surgical TMJ treatment.
  • Presence of considerable pain and/or limited function in the joint area.
  • Clinical and imaging evidence consistent with anatomic joint pathology
  • Previous failure of non-surgical treatment/therapy or a failed implant.
  • High probability of patient improvement by surgical treatment.
  • Patients must be able to return for follow-up examinations.
  • Patients without serious compromising general medical conditions.

排除标准

  • Patients with active infection.
  • Patient conditions where there is insufficient quantity or quality of bone to support the device
  • Patients with perforations in the mandibular fossa and/or bony deficiencies in the articular eminence compromising support for the artificial fossa component.
  • Patients with mandibular and/or zygomatic arch screw holes compromising component fixation
  • Patients requiring partial joint reconstruction or other TMJ procedures not listed as an indication.
  • Patients who are NOT skeletally mature.
  • Patients who are incapable or unwilling to follow postoperative care instructions.
  • Patients who are unable to return for follow-up examinations.
  • Patients with severe hyper-functional habits
  • Patients on chronic steroid therapy.

结局指标

主要结局

Time to Revision

时间窗: 3 years

Time from surgical alloplastic reconstruction of the TMJ to revision surgery (Re-operation or removal)

次要结局

  • jaw pain intensity (VAS score)(1 year, 1.5 years)
  • Interference with eating(1 year, 1.5 years)
  • Maximun Incisal Opening(1 year, 1.5 years)
  • Patient Satisfaction(6 months, 1 year, 1.5 years, and 3 years)

研究者

发起方
Zimmer Biomet
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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