RAHM Foundation Retrospective Study of Various Diseases
2015年2月4日 更新者:Rahm Foundation
Retrospective Registry To Enhance the Understanding of the Variability, Progression and Treatment of Various Disorders
This is a retrospective data collection on treatment of various disorders.
This registry will include a variety of different products, implants, technologies and procedures.
The registry will also collect any adverse events/complications that occur during or following treatment of these conditions.
The data may be utilized to develop strategic treatment pathways and/or benchmarking that will improve patient care.
Ultimately, the goal of the registry is to enhance the understanding of healthcare and the treatment in these disease states.
研究概览
详细说明
The purpose is to collect data on patients with a variety of disorders.
This includes point of care (primary care, internal medicine, pain management providers, etc.) as well as a variety of specialty providers including neurosurgeons, orthopedic surgeons, oncologists, and dermatologists.
The retrospective data collection will consist of a core set of data if available.
The registry will attempt to collect data prior to surgery/treatment/procedures, during surgery, and various time points following surgery/treatment/procedures.
The data will include, but is not limited to demographic data, past medical history, previous treatments, time off of work, type of surgery performed, products/implants/procedures/technology used during surgery, treatments/procedures/technology used for non-surgical conditions, anesthesia used during surgery, complications/adverse events following surgery and or treatment, outcome tools, imaging results, pain assessment, pain medication utilization, length of hospital stay, unplanned hospital admissions, revision surgery, adjacent level disease, genetic testing, urinary drug testing, other diagnostic or assessment testing, patient return to work and patient return to normal activity.
The data collected will vary depending on disease state and treatment.
This registry will also allow for comparisons on different treatments, procedures, etc. with a goal of developing the best pathways for a variety of different disease states.
研究类型
观察性的
注册 (预期的)
10000
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
是的
有资格学习的性别
全部
取样方法
概率样本
研究人群
Patients with various disorders
描述
Inclusion Criteria:
- Subjects who meet eligibility criteria across 1 of the 6 therapeutic areas
Exclusion Criteria:
- Subjects who do not meet eligibility criteria for any of the 6 therapeutic areas
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
---|
Genetic Testing Subjects undergoing genetic testing
|
Topicals Subjects using topical compounds
|
Patients undergoing Spinal Surgery using IOM
|
Spine Patients undergoing cervical or lumbar surgery
|
Total Joint Patients undergoing knee and hip replacement
|
UDT (unrinary drug test) Patients who are given a UDT
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
---|---|
sensory and motor deficits analysis, adverse events, changes in pain, changes in disability, return to work/usual activities, lenttgh of stays, hospital readmission rates, medication compliance rates
大体时间:60 months
|
60 months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2011年1月1日
初级完成 (预期的)
2016年12月1日
研究完成 (预期的)
2016年12月1日
研究注册日期
首次提交
2015年1月29日
首先提交符合 QC 标准的
2015年2月4日
首次发布 (估计)
2015年2月10日
研究记录更新
最后更新发布 (估计)
2015年2月10日
上次提交的符合 QC 标准的更新
2015年2月4日
最后验证
2015年1月1日
更多信息
与本研究相关的术语
其他研究编号
- RAHM 1002 v.6
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.