IRCT2017081635740N1已完成2 期
The efficacy of gabapentin after cesarean section in reducing post-cesarean pain in women with elective cesarean section and spinal anesthesia
Vice Chancellor for research of sabzevar University of Medical Science0 个研究点目标入组 102 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
- 102
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
- 77 years 至 no limit（—）
- 性别
- Female
入选标准
- •Patients who were willing to participate in the study and signed an informed consent letter; age 18 and above; Pregnancy age between 37 and 42 weeks? Term pregnancy; Having a live and monolingual fetus; Auxillary tempreture less than 37.5 degrees; Pfannenstiel incision in the previous cesarean section; Elective cesarean; Spinal anesthesia; No history of seizure; No history of gabapentin susceptibility; No history of psychiatric disorders; No Infectious Disease AIDS and hepatitis; Absence of uncontrolled blood pressure and diabetes; No systemic disease to moderate to severe; No alcohol and drug addiction. Exclusion criteria: Patient's lack of cooperation; Analgesic use 8 hours before surgery; Use of non-steroidal anti-inflammatory drugs 24 hours before surgery; Need for general anesthetic.
排除标准
- 未提供
研究者
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