跳至主要内容
临床试验/CTRI/2026/03/105520
CTRI/2026/03/105520尚未招募不适用

Development and Evaluation of an Alerting System for Critical Biochemical, Microbiological, and Cytological Values in Respiratory Medicine Patients

SIMATS (Saveetha Institute of Medical and Technical Sciences)1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年3月16日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1

研究概览

简要总结

The invention not only improves patient safety by ensuring critical conditions are promptly identified, but it also enhances clinical workflow by reducing the cognitive burden on healthcare providers. It streamlines the process of diagnostic review and helps clinicians to prioritize care based on the severity of the patient’s condition, ultimately improving patient outcomes and reducing the risk of complications. In summary, this invention offers an integrated, automated solution to the challenge of managing complex diagnostic data in respiratory medicine. By combining multiple test results into a unified alerting system, it provides healthcare professionals with timely, actionable insights, thereby enhancing early detection, patient monitoring, and clinical decision making in the management of respiratory diseases. The primary goal of this application is to ensure timely intervention by notifying healthcare providers of any potentially life threatening results. By analyzing diagnostic data, the application can detect deviations from normal values and issue immediate alerts to the relevant medical personnel, enabling them to take swift action. This proactive approach improves response times, reduces the risk of complications, and enhances overall patient outcomes, particularly in critical situations. The system is designed to support clinical decision-making by prioritizing alerts based on the severity of the findings, ensuring that critical values are addressed promptly. It also helps reduce the likelihood of human error and ensures that no critical information is overlooked, especially during busy or high pressure moments in clinical settings. Overall, this application is a vital tool in the efficient management of respiratory patients, promoting patient safety, improving clinical workflows and ultimately leading to better healthcare outcomes.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients aged 18 years and above 2.Individuals diagnosed with respiratory conditions such as chronic obstructive pulmonary disease (COPD), asthma, pneumonia, interstitial lung disease, tuberculosis, or other relevant respiratory pathologies 3.Patients admitted to inpatient wards and intensive care units (ICU) 4.Availability of critical biochemical, microbiological, cytological reports 5.Cases where any biochemical, microbiological, cytological parameters fall within defined critical thresholds that require urgent medical intervention 6.Patients or their legal representatives must provide informed consent to participate in the study.

排除标准

  • 1.Patients under the age of 18 years or those whose age is not documented or unavailable 2.Patients without a primary diagnosis of respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, pneumonia, tuberculosis, interstitial lung disease, lung malignancies etc 3.Patients with incomplete or unavailable laboratory results during the study period 4.Patients or their legal representatives do not provide informed consent.

研究者

发起方
SIMATS (Saveetha Institute of Medical and Technical Sciences)
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

JESVANTHAN E

Saveetha medical college and hospital

研究点 (1)

Loading locations...

相似试验