跳至主要内容
临床试验/CTRI/2025/08/092812
CTRI/2025/08/092812招募中不适用

Precision in Severe Pneumonia Management (PRISM)

Dr Raja Dhar3 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年8月25日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
100
试验地点
3
主要终点
Proportion of patients receiving appropriate antibiotic escalation/de-escalation at 24 hours post randomisation

研究概览

简要总结

Community-acquired pneumonia (CAP) remains a significant cause of ICU admissions worldwide, with viruses contributing substantially to the disease burden. Coinfections with bacteria and viruses further complicate the course and outcomes of patients with viral pneumonia. Pathogen detection rates—and consequently the effectiveness of our empiric regimens, especially concerning drug resistance—remain uncertain. The advent of multiplex PCR techniques with antimicrobial resistance gene detection offers a promising alternative. While these methods provide quicker results and greater sensitivity than conventional techniques, their impact on pragmatic, patient-centered outcomes is still unclear. Evaluating the utility of novel multiplex PCR for pathogen and resistance gene detection within the Indian population is essential. This study aims to determine whether multiplex PCR for severe pneumonia can improve clinical outcomes in our setting.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Adults presenting with severe CAP (as defined by the CURB-65 score 2.BAL in the 1st 72 hrs of admission.

排除标准

  • On palliative care
  • Ventilated at another centre.

结局指标

主要结局

Proportion of patients receiving appropriate antibiotic escalation/de-escalation at 24 hours post randomisation

时间窗: at 24 hours post randomization

次要结局

  • 1.Adults presenting with severe CAP (as defined by the CURB-65 score )

研究者

发起方
Dr Raja Dhar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Raja Dhar

The Calcutta Medical Research Institute

研究点 (3)

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