IRCT20200825048515N60招募中2 期
Comparing the preventive effect of infiltration into the surgical incision bupivacaine with bupivacaine plus dexmedetomidine in reducing pain after caesarean section.
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 80
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
- no limit 至 no limit（—）
- 性别
- All
入选标准
- •Candidate for caesarean section (for the first time)
- •Elective caesarean section
- •The maximum duration of operation is 90 minutes
- •Performing caesarean section surgery using spinal anesthesia or anesthesia from the back
- •Consent to participate in the study
排除标准
- •Uncontrollable underlying disease (ASA3 and higher)
- •Twin pregnancy and above[3]
- •Having a history of allergies to the drugs used (such as bupivacaine, dexmedetomidine)
- •The lack of effect of opioids on them and having acute or chronic pain before surgery
研究者
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