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
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