Adverse reaction event detection method and device in clinical test, medium and equipment

A clinical trial and adverse reaction technology, applied in the field of intelligent medical care, can solve problems affecting the accuracy and reliability of test results, damage to the rights and safety of subjects, serious adverse reaction events, etc., and achieve the detection process of adverse reaction events , Protect rights and security, improve efficiency and timeliness

Inactive Publication Date: 2020-05-12
TIANJIN HAPPY LIFE TECH CO LTD +1
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

During the trial, if protocol deviation (Protocol Deviation, PD) or protocol violation (Protocol Violation, PV, is a relatively serious protocol deviation), adverse reaction events (Adverse Event, AE) or serious adverse reactions may occur Event (Serious Adverse Event, SAE), which damages the rights and safety of subjects, or causes defects in test data, and affects the accuracy and reliability of test results

Method used

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  • Adverse reaction event detection method and device in clinical test, medium and equipment
  • Adverse reaction event detection method and device in clinical test, medium and equipment
  • Adverse reaction event detection method and device in clinical test, medium and equipment

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Embodiment Construction

[0027] Example embodiments will now be described more fully with reference to the accompanying drawings. Example embodiments may, however, be embodied in many forms and should not be construed as limited to the examples set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete and will fully convey the concept of example embodiments to those skilled in the art. The described features, structures, or characteristics may be combined in any suitable manner in one or more embodiments. In the following description, numerous specific details are provided in order to give a thorough understanding of embodiments of the present disclosure. However, those skilled in the art will appreciate that the technical solutions of the present disclosure may be practiced without one or more of the specific details being omitted, or other methods, components, devices, steps, etc. may be adopted. In other instances, well-known technical solution...

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Abstract

The invention provides an adverse reaction event detection method and device in a clinical test, a computer readable storage medium and electronic equipment, and relates to the technical field of intelligent medical treatment. The method comprises the following steps: acquiring original data in a clinical test; standardizing the original data to obtain standardized data; and matching the standardized data by utilizing a rule engine so as to detect adverse reaction events in the clinical test. According to the invention, the adverse reaction event in the clinical test can be accurately and timely detected, so a test team can take correction measures, the clinical test is ensured to be executed along a predetermined scheme, the rights, interests and safety of a subject are protected, and theaccuracy and reliability of a test result are improved.

Description

technical field [0001] The disclosure relates to the field of intelligent medical technology, and in particular to a method for detecting adverse reaction events in clinical trials, a device for detecting adverse reaction events in clinical trials, a computer-readable storage medium, and electronic equipment. Background technique [0002] Clinical trials generally require prior approval and registration, for example, approval from institutions such as IRB (Institutional Review Board, Institutional Review Board). During the trial, if protocol deviation (Protocol Deviation, PD) or protocol violation (Protocol Violation, PV, is a relatively serious protocol deviation), adverse reaction events (Adverse Event, AE) or serious adverse reactions may occur An event (Serious Adverse Event, SAE) that damages the rights and safety of the subjects, or causes defects in the test data, and affects the accuracy and reliability of the test results. [0003] Therefore, there is a need to det...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G16H10/20G06N20/00
CPCG06N20/00G16H10/20
Inventor 郝原艾杰卢璟朱彤
Owner TIANJIN HAPPY LIFE TECH CO LTD
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