Transition of Single Surgeon Bariatric Service to an Interdisciplinary Multiple Surgeon Model
2020年6月13日 更新者:Antonio Barbaro、University of Adelaide
This retrospective study will analyse the transition of an Australian hospital which significantly increased volume of bariatric operations after introduction of a clinical pathway, and to assess the outcomes.
Barriers to introduction of the multidisciplinary pathway and the means to overcome these will also be analysed and discussed.
The analysis will also determine if there are any other areas of bariatric surgery which can be further investigated to optimise current practice.
研究概览
地位
完全的
研究类型
观察性的
注册 (实际的)
146
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
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients who underwent bariatric surgery at the Queen Elizabeth Hospital (South Australia) between the years of 2008 and 2018.
描述
Inclusion Criteria:
- Participants must have had bariatric surgery at The Queen Elizabeth Hospital between 2008-2018
Exclusion Criteria:
- nil
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 |
干预/治疗 |
|---|---|
|
2008-2012 Participants
Participants who underwent bariatric surgery between 2008 and 2012 (inclusive).
|
|
|
2013-2016 Participants
Participants who underwent bariatric surgery between 2013 and 2016 (inclusive).
|
|
|
2017- 2018 Participants
Participants who underwent bariatric surgery between 2017 and 2018 (inclusive).
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Post-operative length of stay (nights)
大体时间:The number of nights the participant stay in hospital from the day of procedure to the day of hospital discharge. This time period occurs immediately after the procedure. This data will be retrospectively reviewed on an average of 5 years.
|
This will be measured in number of nights the participant stayed in hospital after the procedure.
|
The number of nights the participant stay in hospital from the day of procedure to the day of hospital discharge. This time period occurs immediately after the procedure. This data will be retrospectively reviewed on an average of 5 years.
|
|
End weight loss
大体时间:Up to 12 months
|
Post-operative weight loss
|
Up to 12 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
End weight loss
大体时间:Up to 24 months
|
Post-operative weight loss
|
Up to 24 months
|
|
End weight loss
大体时间:Up to 36 months
|
Post-operative weight loss
|
Up to 36 months
|
|
Intraoperative time
大体时间:The start time of the operation to the end time of the procedure. This data will be retrospectively reviewed on an average of 5 years.
|
Duration of operative time measured in minutes
|
The start time of the operation to the end time of the procedure. This data will be retrospectively reviewed on an average of 5 years.
|
|
Post-operative complications
大体时间:Up to 36 months
|
Complications which occurred in the post operative period
|
Up to 36 months
|
|
Number of operations performed in time period
大体时间:Retrospectively reviewed, 1 yearly
|
The number of operations which occurred in each group
|
Retrospectively reviewed, 1 yearly
|
|
Type of Operation Performed
大体时间:Retrospectively reviewed, 1 yearly
|
The number of the different types of bariatric operations which occurred in each group
|
Retrospectively reviewed, 1 yearly
|
|
Number of participants converted from Gastric Sleeve to Gastric Bypass
大体时间:Retrospectively reviewed, 1 yearly
|
Retrospectively reviewed, 1 yearly
|
|
|
Number of patients on surgical waitlist
大体时间:Retrospectively reviewed, 1 yearly
|
The number of patients on the surgical waitlist for each time period
|
Retrospectively reviewed, 1 yearly
|
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。
调查人员
- 首席研究员:Antonio Barbaro, MBBS、University of Adelaide
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 (实际的)
2008年1月1日
初级完成 (实际的)
2018年12月31日
研究完成 (实际的)
2020年6月3日
研究注册日期
首次提交
2020年6月4日
首先提交符合 QC 标准的
2020年6月11日
首次发布 (实际的)
2020年6月16日
研究记录更新
最后更新发布 (实际的)
2020年6月16日
上次提交的符合 QC 标准的更新
2020年6月13日
最后验证
2020年6月1日
更多信息
与本研究相关的术语
其他研究编号
- 13204
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.