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临床试验/CTRI/2024/08/072557
CTRI/2024/08/072557尚未招募不适用

Evaluation of Accuracy of Ultrasound guided airway assessment and clinical parameters in prediction of difficult airway - A prospective analytical Observational study

DR Amrutha D1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年8月28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
150
试验地点
1
主要终点
Airway assessment using clinical parameters and ultrasonographic parameters

研究概览

简要总结

This study is a prospective analytical observational study for evaluating the accuracy of ultrasound guided airway assessment and clinical parameters in prediction of difficult airway. Routine clinical parameters like h/o snoring, MMPC, ULBT, TMD(CMS), NC (CMS), HMD(CMS),SMD(CMS) will be measured. ultrasonographic measurements like ANS - VC, STB + TT, SED, SHD will be measured. On the day of surgery, theatre will be kept ready. Patient will be connected to standard monitors.18G IV cannula will be secured. After preoxygenation and premedication , all the patients will be induced with inj.propofol – 2mg/kg, post check ventilation, inj.vecuronium -0.1mg/kg will be administered. Patient will be given sniffing position ,direct laryngoscopy will be performed using appropriate sized Macintosh blade and intubated  with endotracheal tube by the same Anaesthesiologist.•        Difficult mask ventilation and intubation difficulty scale (IDS) will be noted by the investigator.

•        Anaesthesia will be maintained as per standard procedures. In case of unanticipated Cannot Ventilate / Cannot Intubate, difficult airway algorithm will be followed.

 With the help of the above collected data i.e, ultrasonographic airway assessment and clinical parameters ,the accuracy of the same and their validity in predicting the difficult airway will be assessed ,which may help for proper planning and management of safe securing of airway.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Adult patients 18- 65yrs requiring general anaesthesia with ET intubation for elective surgeries All gender Patients who have given valid informed consent Upper lip bite test less than II Interincisor gap more than 3 centimetres Patients with adequate neck movements.

排除标准

  • Any patient planned for awake fiberoptic intubation Edentulous patients/dentures.
  • Patients with facio maxillary trauma , facial anomalies Patients with restricted neck movements, neck swellings Obstetric patients Emergency surgeries Cervical spine injury/pathology Rapid sequence intubation H/O difficult airway in previous surgery.

结局指标

主要结局

Airway assessment using clinical parameters and ultrasonographic parameters

时间窗: Preoperatively in the pre assessment clinic on the day prior to surgery

次要结局

  • To find the prevalance of difficult intubation(To find difficult mask ventilation score & intubation difficulty scale during induction on the day of surgery)

研究者

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

Dr Amrutha D

Sri Muthukumaran Medical College hospital and Research Institute

研究点 (1)

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