跳至主要内容
临床试验/CTRI/2025/07/091424
CTRI/2025/07/091424尚未招募Phase 3 4

Supra and subglottic instillation of dexmedetomidine for prevention of coughing during emergence from general anaesthesia : A comparison with lignocaine .

DR HARSHA1 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
170
试验地点
1
主要终点
To assess the incidence and severity of coughing during emergence from general anesthesia

研究概览

简要总结

So far no study has detected the  local action of dexmedetomidine on tracheal mucosa in patients undergoing endotracheal intubation. Therefore we hypothesize that direct instillation of dexmedetomidine via supra/subglottic injectable endotracheal tube port could suppress cough reflex following tracheal extubation.

This prospective, randomized, double blinded trial will compare the safety and efficacy of direct instillation of tracheal mucosa by dexmedetomidine and lidocaine via a supra or subglottic injectable endotracheal port forsmooth tracheal extubation in patients undergoing general surgery.

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

  • Consent for participation
  • Scheduled for elective surgery under genaral anaesthsia.

排除标准

  • Refusal of Patient.
  • With Known contraindication and sensitivity of study drugs
  • History of asthma or COPD
  • Who requires post op ventilation
  • Anticipated difficult airway
  • history of tracheal surgery.

结局指标

主要结局

To assess the incidence and severity of coughing during emergence from general anesthesia

时间窗: Time POINT - JUST AFTER EXTUBATION, 1min post extubation, 2 min post extubation, 3 min post extubation, 4 min post extubation, 5 min post extubation

次要结局

  • 1. Extubation Time(2. Hemodynamic Parameters)

研究者

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

DR HARSHA

INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES

研究点 (1)

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