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临床试验/CTRI/2024/12/077684
CTRI/2024/12/077684已完成不适用

USE OF VIDEOLARYNGOSCOPY AND VIDIAC (VIDEOLARYNGOSCOPIC INTUBATION AND DIFFICULT AIRWAY CLASSIFICATION) SCORE FOR PREDICTING VIDEOLARYNGOSCOPE ASSISTED DIFFICULT INTUBATION IN PATIENTS - A PROSPECTIVE OBSERVATIONAL STUDY

self1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2024年12月16日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
96
试验地点
1
主要终点
To correlate VIDIAC score attained during videolaryngoscopy with cormack lehane grade in detecting difficult intubations

研究概览

简要总结

Effective airway management is the cornerstone of perioperative patient safety. Difficult airway remains a common challenge for Anesthesiologists, Intensivists, Emergency physicians and Otolaryngologists. Treating patients with difficult airway following an airway management algorithm helps to reduce the incidence of airway-related complications. Anesthesiologists as well as a range of professionals should develop appropriate strategies according to their own experience, patient status, type of surgery and available airway devices to achieve reliable preoperative evaluation and effective intraoperative monitoring to maximize the degree of patient safety. This study is planned to evaluate the patient’s airway for assessing the difficulty associated with the intubation using videolaryngoscopy and establishing a VIDIAC score for labelling the cases of  difficult intubation and hence enabling the concerned clinicians to have proper strategy during procedures in future in order to avoid complications and minimize morbidity..

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

  • ASA status 1 to 3 SARI score more than or equal to 4.

排除标准

  • Pregnant women Patients in whom awake intubation is planned SARI score less than 4.

结局指标

主要结局

To correlate VIDIAC score attained during videolaryngoscopy with cormack lehane grade in detecting difficult intubations

时间窗: Baseline 4 weeks and 16 weeks

次要结局

  • To compare VIDIAC score with Simplified Airway Risk Index score(SARI score)(Baseline, 8 weeks & 16 weeks)

研究者

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

Thota Sridhar

Command Hospital(EC), kolkata

研究点 (1)

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