跳至主要内容
临床试验/NCT06911463
NCT06911463Enrolling By Invitation不适用

Conscious Sedation With Suprainguinal Facia Iliaca Block Versus Ilioinguinal Iliohypogastric Block for Transcatheter Aortic Valve Implantation (TAVI)

Ain Shams University1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2025年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
45
试验地点
1
主要终点
The primary outcome is the timing to the first rescue analgesia

研究概览

简要总结

the aim of the present study is to compare suprainguinal fascia iliaca block and ilioinguinal-iliohypogastric (II-IH) nerve block in improving the quality of conscious sedation, including reducing patients' requirements for analgesia also better satisfaction for both patient and surgeon as regards patient outcome and decreasing the incidence of conversion to general anesthesia during TAVI procedure

研究设计

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

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •aged >20 years with severe aortic stenosis undergoing elective, non-emergent, non-urgent transfemoral Sapien 3TM (Edwards Lifesciences Corp., Irvine, CA, USA) or CoreValveTM (Medtronic, Minneapolis, MN, USA) implantation were included in the study

排除标准

  • •younger than 20 years

研究组 & 干预措施

Group I (F)

Active Comparator

suprainguinal fascia iliaca block group (SIFIB)

干预措施: suprainguinal fascia iliaca block group (SIFIB) (Other)

Group II (I)

Active Comparator

iliohypogastric and ilioinguinal group (IL-IH)

干预措施: iliohypogastric and ilioinguinal group (IL-IH) (Other)

Group III (C)

Other

control group patients received infiltration of 0.5% 10ml bupivacaine and 1% 10 ml lidocaine in the groin at the site of puncture

干预措施: Local infiltration (Other)

结局指标

主要结局

The primary outcome is the timing to the first rescue analgesia

时间窗: Six months

sedation score (RASS), and pain (numerical rating scale \[NSR\] from 0 \[no pain\] to 10 \[unbearable pain\]) at 0 time start of sedation and every 30 min till the end of the procedure then 1, 3, and 6 h after TAVI. While, Pain intensity was assessed using numeric rating scale (NRS 0-10; 0 = no pain; 10 = the worth pains imaginable) in five time-points intraoperatively (femoral artery cannulation (1), aortic valve system introduction (2), aortic valve system removal (3), vessel closure devices insertion (4), the end of the operation (5)). In addition, the need for post TAVI pacing, vascular complications at the TAVI access site during admission, and the length of hospital stay were recorded. Rescue analgesia will be given When NRS was more than 4, patient discomfort or doctor dis-satisfaction is detected, 0.5 mic /kg fentanyl will be given. The primary outcome is the timing to the first rescue analgesia

次要结局

未报告次要终点

研究者

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

Mohammed Shabayek

Lecturer of Anesthesia, ICU and pain management

Ain Shams University

研究点 (1)

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