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临床试验/TCTR20220430008
TCTR20220430008已完成2 期

Effects of different doses of fentanyl combined with bupivacaine in spinal anesthesia elective cesarean section: a randomized clinical trial in the Palestinian obstetrics practice

An-Najah National University0 个研究点目标入组 160 人开始时间: 2022年4月30日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
160

研究概览

简要总结

The women who received 25 mcg of fentanyl with 7.5 mg of hyperbaric bupivacaine had significantly shorter sensory block latency, longer duration of sensory block, longer duration of analgesia, less need for rescue analgesia, expressed higher satisfaction with analgesia, experienced less hemodynamic instabilities, and experienced fewer episodes of bradycardia and vomiting compared to those who received bupivacaine alone or in combination with lower doses of fentanyl.

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

  • 1) being at least 18 years old, 2) full-term pregnancy (at least 37 weeks), 3) pregnant with a single fetus, 4) being scheduled for caesarian delivery under spinal anesthesia, 5) American Society of Anesthesiologists (ASA) physical class I and II, and 6) providing written informed consent.

排除标准

  • Women who had a history of sensitivity/allergy for local anesthetics and opioids, psychiatric disorders, drug addiction, pregnancy complications, fetal distress, and/or those who could not provide written informed consent were excluded.

研究者

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