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临床试验/IRCT201603155596N3
IRCT201603155596N3已完成未知

Comparison of Ondansetron and PC6 acupressure point on postoperative nausea and vomiting in patients, undergone elective cesarean section in 2016; a randomized clinical trial

orestan University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
120

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

年龄范围
18 years 至 45 years(—)
性别
Female

入选标准

  • elective cesarean; being NPO 8 to 12 hours before surgery; being NPO 6 hours after surgery; lack of symptomatic digestive disease; lack of motion sickness; lack of dizziness; lack of cardiovascular disease; lack of pulmonary disease; lack of middle ear disease; lack of diabetes; lack of infectious disease; lack of fever; lack of hypertension; lack of lateral surgery except for cesarean; lack of carpal tunnel syndrome; not taking alcohol; not taking immunosuppressive drugs; lack of long or unusual bleeding; lack of hemoglobin level less than 10 mg/dl; not receiving drugs except for antibiotics and analgesics in form of Diclofenac suppository daily 6 hours after surgery; American Society of Anesthesiologists classes I and II patients; patients with mild diseases without any performance limitation; patients with controlled disease; controlled diabetes or hypertension without systemic effects; smoking without chronic obstructive pulmonary disease; mild obesity; pregnant women aged 18 to 45 years with 38 to 40 weeks pregnant; exclusion criteria: lack of desire to continue cooperation in each step of research; change in surgery trend such as needing to general anesthesia; outbreak of any problem and uncommon and unexpected complication; severe nausea and vomiting according to anesthesiologist’s diagnosis; emergency cesarean; having lateral surgery except for cesarean; the weight more than 100 kg and less than 50 kg.

排除标准

  • 未提供

研究者

发起方
orestan University of Medical Sciences

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