跳至主要内容
临床试验/CTRI/2019/09/021157
CTRI/2019/09/021157尚未招募未知

Comparison of efficacy of palonosetron - dexamethasone combination with palonosetron or dexamethasone alone for prophylaxis against post operative nausea and vomiting in patients undergoing middle ear surgery

Department Of Anesthesiology And Critical Care0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients Belonging To American Society Of Anaesthesiology(ASA) Grade 1 And 2 , And Of Age Group 18 TO 60 Years With Body Weight 40 TO 80 Kg Of Either Sex Undergoing Middle Ear Surgery And Willing To Give A Written And Informed Consent.

排除标准

  • 1 Pregnant and lactating females or patients having huge abdominal mass or tumour.
  • 2 A cancer patient who has had chemotherapy within 4 weeks prior to study entry (Screening visit) or any kind of emetogenic radiotherapy within 8 weeks prior to study entry (Screening visit).
  • 3 Patients who had received any investigational drugs within 30 days before study entry or taken any drug with potential antiemetic efficacy within 24 hours prior to anaesthetic procedures.
  • 4 Patients who have history of any vomiting, retching, or nausea in the 24 hours preceding the administration of anaesthesia.
  • 5 Patients who have current history of alcohol abuse or drug abuse or taking any hormonal supplements.
  • 6 Patients having hypersensitivity/contraindication to 5-HT3 antagonists or study drug.
  • 7 Patients having cardio respiratory dysfunction or renal, hepatic or metabolic derangements or history of epilepsy.
  • 8 Patients with Ryleâ??s tubes in situ.
  • 9 Patients in varying degrees of shock during pre and post operative period.
  • 10 Patients who will require any opioid analgesic for post operative pain relief during the period of study.

研究者

发起方
Department Of Anesthesiology And Critical Care

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