A prospective randomised double blinded study to compare efficacy of two different doses of dexmedetomidine for attenuation of pressor responses to laryngoscopy and endotracheal intubation under bispectral index- controlled general anaesthesia

JLN Medical College Ajmer0 个研究点目标入组 120 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•Age group between 18 and 55 years.
•Body weight 50 to 70 kg.
•Patients belonging to ASA (American Society of Anaesthesiologists) physical status class-I and II.
•Patients undergoing elective surgeries under general anaesthesia.

•Patientâ??s refusal.
•Uncooperative patients.
•Any known hypersensitivity or contraindication to Dexmedetomidine.
•History of convulsion, bleeding disorder, severe neurological deficit, thyroid disorder.
•Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above).
•Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
•Anticipated difficult airway which requires >20seconds to intubate.

发起方

JLN Medical College Ajmer