NCT01357187已完成不适用
An Evaluation of the Effect of the AmnioFix™ Amniotic Membrane Allograft on Scar Tissue and Adhesions in Patients Undergoing Posterior Instrumentation Removal
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Tenacity and frequency of soft tissue adhesion
研究概览
简要总结
The objective of this study is to evaluate the clinical effectiveness of AmnioFix™ in the reduction of the tenacity and frequency of soft tissue adhesions during the removal of segmental posterior lumbar instrumentation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults (18 years or older)
- •Diagnosed with lumbar pathology requiring elective lumbar interbody fusion
- •Willingness to comply to follow-up examinations and diagnostic imaging procedures
- •Ability to give full written informed consent
排除标准
- •Previous surgical procedure performed at same site
- •Sign or symptoms of other disease which could result in allograft failure
- •Require a corpectomy
- •Participating in another drug or device clinical trial
- •Pregnant or may become pregnant during the study
- •Involved in workmen's compensation or other litigation relative to a spine injury
- •Past medical history of allograft implantation which resulted in graft failure
- •Any condition requiring treatment above the normal standard of care
- •Currently taking medications which could affect graft incorporation (supervising physicians discretion)
- •Auto-Immune disease
- •Renal failure
- •Failure to sign or understand informed consent information
- •History of drug and/or alcohol abuse
- •Allergic to aminoglycosides
结局指标
主要结局
Tenacity and frequency of soft tissue adhesion
时间窗: At the time of removal of segmental posterior lumbar instrumentation
次要结局
- Presence and extent of scar tissue using histological analysis of the lumbar tissue adjacent to the surgical site(At the time of removal of segmental posterior lumbar instrumentation)
- Number of intra-operative complications(At the time of removal of segmental posterior lumbar instrumentation)
研究者
研究点 (2)
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