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临床试验/NCT05172882
NCT05172882已完成不适用

Comparison of the Efficacy of Transversalis Fascia Plane Block and Wound Infiltration in Varicoselectomy Surgery; Randomised, Controlled Study.

Ataturk University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年11月15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
60
试验地点
1
主要终点
Pain Scores (0 (low)-10 (high))

研究概览

简要总结

Before surgery, patients will be divided into 2 groups as transversalis fascia plane block will be applied and skin infiltration will be applied. Post-operative analgesic procedures will be applied to patients receiving general anesthesia. Postoperative analgesic consumption and pain scores of the patients will be evaluated.

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
Single (Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Patients over the age of 18 who will undergo Varicocele operation

排除标准

  • •Patients with allergic reaction to anesthesia and analgesia drugs to be used
  • •Patients who did not want to voluntarily participate in the study
  • •Severe systemic disease (kidney, liver, pulmonary, endocrine)
  • •Substance abuse history
  • •Chronic pain history
  • •Psychiatric problems and communication difficulties
  • •History of hematological problem
  • •Patients with severe hemodynamic instability due to infection, heavy bleeding

研究组 & 干预措施

Wound Infiltration

Experimental

Wound infiltration will be applied to the surgical incision site for patients in this group. Infiltration fluid will contain 20 ml 0.25% bupivakain.

干预措施: Wound site infiltration (Procedure)

Transversalis Fascia Plane Block

Experimental

Transversalis fascia plane block will be performed on only one periinguinal side for patients in this group. Block fluid will contain 20 ml 0.25% bupivakain.

干预措施: Transversalis fascia plane block (Procedure)

结局指标

主要结局

Pain Scores (0 (low)-10 (high))

时间窗: 24th hour

Pain will be assessed by visual analog scale scores

Pain Scores (0 (low)-10 (high))

时间窗: 1st hour

Pain will be assessed by visual analog scale scores

Pain Scores (0 (low)-10 (high))

时间窗: 2nd hour

Pain will be assessed by visual analog scale scores

Pain Scores (0 (low)-10 (high))

时间窗: 4th hour

Pain will be assessed by visual analog scale scores

Pain Scores (0 (low)-10 (high))

时间窗: 8th hour

Pain will be assessed by visual analog scale scores

Pain Scores (0 (low)-10 (high))

时间窗: 12th hour

Pain will be assessed by visual analog scale scores

次要结局

  • Rescue analgesic consumption(Any time on postsurgical first 24 hour.)

研究者

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

Erkan Cem ÇELİK

Associate Professor

Ataturk University

研究点 (1)

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