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临床试验/NCT06076096
NCT06076096已完成不适用

Ultrasound-Guided Supra-Inguinal Fascia Iliaca Block As an Anesthesia Method for Lower Extremity Surgeries: A Single-Center Retrospective Cohort Feasibility Study

Samsun University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
16
试验地点
1
主要终点
Block Success which provided surgical anesthesia, intraoperatively

研究概览

简要总结

The Ultrasound-guided Supra-inguinal Fascia Iliaca Block (SIFIB) is an advanced regional anesthesia technique strategically directed at the three primary nerves of the lumbar plexus. As the scope of regional anesthesia methods continues to grow in clinical application, this approach emerges as a versatile method. It can be used independently for pain management or as the primary anesthetic method, particularly in well-selected patients undergoing isolated limb surgeries or in combination with other regional anesthesia approaches.

详细描述

The study follows a retrospective cohort feasibility design, conducted within the confines of a tertiary hospital. The requisite data for analysis was acquired by accessing patient records and electronic data systems. A cohort of 16 patients was carefully chosen for inclusion in the study, and the administration of blocks was carried out before the surgical procedures.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ASA I-III patients who underwent elective lower limb surgical procedures.

排除标准

  • Patients who received general anesthesia, neuraxial anesthesia, or infiltration anesthesia were excluded.

结局指标

主要结局

Block Success which provided surgical anesthesia, intraoperatively

时间窗: Intraoperatively and PACU unit (up to 2 hours)

After performing the blocks, the sensory block was examined with a pinprick test using a 27-gauge hypodermic needle, (0 = no sensory block; 1 = tactile sense present, no pain; 2 = no tactile sense and no pain). Cases with a score of 1 or 2 after 30 min were considered successful.

次要结局

  • Additional analgesic requirement(Intraoperatively and PACU unit (up to 2 hours))

研究者

发起方
Samsun University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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