跳至主要内容
临床试验/CTRI/2026/02/105030
CTRI/2026/02/105030尚未招募不适用

Prospective study of critical events during anaesthesia for non-operating room procedures in oncology patients

ACTREC, TMC1 个研究点 分布在 1 个国家目标入组 2,100 人开始时间: 2026年3月10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
2,100
试验地点
1

研究概览

简要总结

Prospective Study of Critical Events During Anaesthesia for Non-Operating Room Procedures in Oncology Patients.

This study aims to evaluate the incidence, nature, and contributing factors of critical events during non-operating room procedures in cancer patients, with the goal of enhancing peri-procedural safety and aligning practice with the unique needs of this vulnerable population. It will be a  prospective observational study done over a period  of 6 months. We will recruit all elective and emergency patients posted on the same day for a diagnostic or a therapeutic procedure under General Anaesthesia /sedation at all the following non- operating room procedures (CT scan, MRI suite, radiation therapy, interventional radiology, proton beam therapy, endoscopy suite, bone marrow procedure room and minor OT room). The critical events in all the elective and emergency non-operative procedures requiring anaesthesia (general anaesthesia/ monitored anaesthesia care) will be recorded. We intend to capture timing of occurrence of the event, type of event (airway/ respiratory/ haemodynamic changes / allergy, incorrect drug use/ drug error) action taken and patient outcome. The critical events are pre-defined based on established literature. The case record forms will be filled for each patient done under anaesthesia (general anaesthesia/

monitored anaesthesia care) by the anaesthetists of the designated location. The case record forms will be received at the end of the day by the primary investigators, co-investigators and research nurse to record the events.  Data collection will be anonymised and data will be securely stored. Descriptive statistics will be used to summarize baseline characteristics, with continuous variables presented as mean +/- standard deviation (SD) and categorical variables as frequencies and percentages. Logistic regression analysis will be done to identify significant factors associated with post procedure complications.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • All elective and emergency patients undergoing a diagnostic or a therapeutic procedure under general anaesthesia/sedation at one of the following locations: -CT scan -MRI suite -Radiation therapy -Interventional radiology -Proton beam therapy -Endoscopy suite -Bone marrow procedure room -Minor OT room.

排除标准

  • Patients with incomplete case records required for incident analysis.
  • Patients not receiving anaesthesia care.
  • Patients undergoing procedures outside the defined study areas mentioned in the inclusion criteria.

研究者

发起方
ACTREC, TMC
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Ashwini Rane

ACTREC, TMC, HBNI

研究点 (1)

Loading locations...

相似试验