跳至主要内容
临床试验/CTRI/2024/06/069618
CTRI/2024/06/069618已完成2/3 期

Comparative evaluation of efficacy of add on chlorhexidine with lignocaine gargles for prevention of post operative sore throat after ambu auragain laryngeal mask airway insertion

Dayanand Medical College and Hospital1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2024年7月6日最近更新:

试验速览

阶段
2/3 期
状态
已完成
发起方
入组人数
160
试验地点
1
主要终点
To compare the Incidence and severity ( subjective grading score ) of sore throat in Group C (lignocaine +chlorhexidine) and Group

研究概览

简要总结

Post operative sore throat is one of the most common post-operative

complication with an incidence of 65%. Many pharmacological and non

pharmacologicaltherapeutic measures have been tested to prevent POST with variable

results. We used AmbuAuragaineLMA in this study as it is easy to insert,less invasive and is

associated with minimal haemodynamic response and fewer complications compared to ETT.

A total of 160 adult patients (18-65 years age) ASA I,II and III

undergoing surgery in general anaesthesia with Ambu Auragain LMA will be enrolled in this

prospective randomized study.Patients will be allocated into two groups Group C (viscous

lignocaine+chlorhexidine) and Group L (viscous lignocaine+normal saline) of 80 patients each.list.Group C will receive 15ml of 2% xylocaine

viscous with 5 ml chlorhexidine and group L will receive 15ml of 2% xylocaine viscous with 5

ml normal saline as gargle solution 15 minutes before the induction of anaesthesia for 30

seconds. In the operation theatre after standard anaesthesia induction Ambu Auragain LMA

will be inserted. Incidence of post-operative sore throat will be evaluated using a 4- point scale

at 0h,1h,2h,4h,12h and 24h in post anaesthesia care unit (PACU).

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

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

入选标准

  • 1 Adult patients of age 18-65 years of either sex posted for elective procedure not more than 3 hours duration under general anaesthesia with AmbuAuragain LMA.
  • 2 American Society Of Anaesthesiologists (ASA) status I, II and III.

排除标准

  • 1 Smokers 2 Any known contraindication or hypersensitivity to study drugs.
  • 3 Preoperative sore throat 4 Upper or lower respiratory tract infection 5 Anticipated difficult intubation 6 Risk of aspiration(full stomach, history of gastroesophageal reflex disease, hiatus hernia) 7 Morbid obesity ; BMI > 35 kg/m2 8 Derranged coagulation.

结局指标

主要结局

To compare the Incidence and severity ( subjective grading score ) of sore throat in Group C (lignocaine +chlorhexidine) and Group

时间窗: In the postanaesthesia care unit (PACU), all patients will be evaluated for post operative sore throat at 0,1, 2, 4, 12 and 24 hrs

L (lignocaine + Normal saline).

时间窗: In the postanaesthesia care unit (PACU), all patients will be evaluated for post operative sore throat at 0,1, 2, 4, 12 and 24 hrs

次要结局

  • Post operative side effects if any like nausea/vomiting , sedation,bleeding from oral cavity will be noted.(24 hours)

研究者

发起方
Dayanand Medical College and Hospital
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Kamakshi Garg

Dayanand Medical College and Hospital

研究点 (1)

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