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临床试验/JPRN-UMIN000016847
JPRN-UMIN000016847已完成未知

Prevention of post operative nausea and vomiting with dexamethasone in children and adolescents undergoing posterior spinal fusion for adolescent idiopathic scolioses : A randomized double-blind clinical trial - Prevention of post operative nausea and vomiting with dexamethasone in children and adolescents undergoing posterior spinal fusion for adolescent idiopathic scolioses : A randomized double-blind clinical trial

Department of Anesthesiology, Keio University School of Medicine0 个研究点目标入组 100 人开始时间: 2015年5月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

研究概览

简要总结

The 72 h incidence of PONV was significantly lower in the dexamethasone group than in the control group (62.5% vs 84.0%; RR 0.74, 95% CI 0.58-0.96, P=0.02). During the first and second 24 h postoperative intervals, fewer patients in the dexamethasone group received rescue antiemetics. Visual analogue scale scores for nausea and pain were lower in the dexamethasone group than in the control group during the first 24 h postoperatively. Dexamethasone did not increase the number of adverse events. The results of this study showed that a single dose of dexamethasone was effective for reducing PONV after paediatric scoliosis correction surgery.

研究设计

研究类型
Interventional

入排标准

年龄范围
10years-old 至 20years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Contraindication to the use of any of the study medications. Patients who took steroids or immunosuppressant within 1 month prior to the surgery. Patients who took antiemetics within 24h prior to the surgery.

研究者

发起方
Department of Anesthesiology, Keio University School of Medicine

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