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临床试验/IRCT2016081726861N2
IRCT2016081726861N2已完成2 期

The Comparison of the Effect of Lavender Essence and Chamomile Essence on pain severity after cesarean section under spinal anesthesia: A blind placebo-controlled randomized clinical trial.

Vice Chancellor for research and technology of Kurdistan University of Medical Sciences0 个研究点目标入组 129 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
129

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 35 years(—)
性别
Female

入选标准

  • Inclusion criteria included: Cesarean section candidates (after surgery); being volunteer to participate in the study; lack of underlying medical conditions (diabetes, chronic respiratory disease, chronic heart disease, kidney or liver disorders and other acute or chronic disorders); surgery under spinal anesthesia; Get 100-mg diclofenac suppository in the recovery room; getting more than three scores of pain severity using the visual analog scale after surgery. Exclusion criteria included Patient’s unwillingness from continuing the study, and unpredicted events after surgery such as cardiac arrest or patient’s death.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research and technology of Kurdistan University of Medical Sciences

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