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临床试验/NCT03741452
NCT03741452已完成不适用

Evaluation of Ultrasound-guided Transversalis Fascia Plane Block for Postoperative Analgesia in Cesarean Section: A Prospective, Randomized, Controlled Clinical Trial

Maltepe University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年11月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
2
主要终点
24 hours tramadol consumption

研究概览

简要总结

Transversalis fascia plane block is a regional anesthesia technique described ten years ago. Its use for many indications has been identified by case reports in the literature. As the investigators have considered that transversalis fascia plane block could be efficacious for providing postoperative analgesia in the cesarean section, the investigators have implemented the application of this blockade into practice at the clinic. The main purpose of this study is to evaluate the analgesic effect of ultrasound-guided bilateral transversalis fascia plane block in cesarean section.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • patients undergoing cesarean section under general anesthesia ASA I-II

排除标准

  • patients undergoing cesarean section under neuraxial anesthesia morbidly obesity ASA III - IV infection of the skin at the site of needle puncture area patients with known allergies to any of the study drugs coagulopathy recent use of analgesic drugs

研究组 & 干预措施

Transversalis fascia plane block

Experimental

The transversalis fascia plane block will be administrated to this group at end of the surgery under general anesthesia. An intravenous patient-controlled analgesia device within tramadol will be given to the patients postoperatively.

干预措施: transversalis fascia plane block (Other)

Control group

No Intervention

In this group, patients will receive only multimodal analgesic treatment including patient-controlled analgesia with tramadol. No block will be performed.

结局指标

主要结局

24 hours tramadol consumption

时间窗: 24 hour

tramadol consumptions for both group will be recorded

次要结局

  • Numeric rating scale for postoperative pain intensity(24 hours)
  • Postoperative nausea and vomiting(24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Asst. Prof. Serkan Tulgar, M.D.

assoc professor in anesthesiology and reanimation

Maltepe University

研究点 (2)

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