跳至主要内容
临床试验/NCT03527407
NCT03527407已完成不适用

MIDAS: Minimal-dataset for the Assessment of Surgical Outcomes - Potential in Hip Surgery (ch18Jakob3)

University Hospital, Basel, Switzerland1 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2017年7月1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
入组人数
146
试验地点
1
主要终点
Changes to Baseline in the generic scores EuroQuol5 (EQ-5D)

研究概览

简要总结

Swiss legislation requires health service providers to collect such information. of medical quality indicators as part of the quality and performance audit (Article 22a KVG). In addition, comparisons of clinics or specialist specialists on cost and quality of results are required (Art. 49 (8)).

Currently, the quality of a medical therapy is evaluated rather negatively on the absence (or occurrence) of complications. In contrast, however, the goal of therapy must be to improve or maintain the health-related quality of life (HRQoL). Accordingly, the Swiss Society of Surgery (SGC-SSC), in collaboration with the Association for Quality Assurance in Surgery (AQC), has developed a minimum dataset designed to assess the quality of life of patients after surgical intervention. In order to enable Switzerland to be comparatively independent of the discipline, generic (in the Research Plan - MIDAS -V2, date 24.05.2017 Page 5/57 Contrary to disease-specific) survey instruments proposed that cover the general quality of life in its different facets, regardless of the function of individual organ systems. The complication documentation was not completely abandoned in this proposal, but is only a quality indicator among many due to patient-related outcome measurements.

However, the development of a minimal data set with quality indicators that are applicable across all surgical sub-disciplines for evaluating the quality of treatment of acute and chronic diseases raises a number of fundamental questions that can only be answered to a limited extent without empirical studies. Five essential questions are:

I. Is it sufficient to work with generic quality of life tools or is it necessary to use disease / indication specific instruments or functional tests? II. Which is the best, solid time for a follow-up? III. Is it possible and useful to make a third-party determination of the quality of life in patients with limited cognitive abilities? IV. Which preoperative risk factors should be documented so that sufficient adjustment for case mix differences in hospital comparisons can be made? V. Which perioperative and postoperative factors, in particular complications, must be raised beyond the quality of life, as they reflect an independent aspect of quality?

研究设计

研究类型
Observational
观察模型
Case Only
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
否

入选标准

  • •Standard therapy of one of the following diagnoses
  • •Femoral neck fracture after low-energy trauma (implantation of a head endoprosthesis)
  • •Coxarthrosis (implantation of a total hip prosthesis)

排除标准

  • •Rejection of study participation or standard therapy
  • •Patients who are unlikely to attend routine follow-up (e.g., tourists)
  • •Patients in palliative care
  • •Malignancy (known or diagnosed in the course of time)
  • •Patients with a limited knowledge of German, who can answer the questionnaire even with the help of a study nurse seems unrealistic
  • •Participation in an interfering clinical intervention study within the last three months
  • •persons unable to consent (long-term incapacity to consent)

结局指标

主要结局

Changes to Baseline in the generic scores EuroQuol5 (EQ-5D)

时间窗: baseline, month 3 and month 12

The degree of mapping the influence of known factors for the quality of therapy to changes to Baseline in the generic scores EuroQuol5 (EQ-5D). different measuring times between 3 and 12 months.

Changes to Baseline in the Health Utility Index Mark 3 (HUI3)

时间窗: baseline, month 3 and month 12

The degree of mapping the influence of known factors for the quality of therapy to changes to Baseline in the Health Utility Index Mark 3 (HUI3). different measuring times between 3 and 12 months.

次要结局

未报告次要终点

研究者

发起方
University Hospital, Basel, Switzerland
申办方类型
Other
责任方
Sponsor

研究点 (1)

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