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临床试验/NCT05094323
NCT05094323已完成2 期

Analgesic Efficacy of Ultrasound-Guided Deep Serratus Anterior Plane Block, Local Wound Infiltration, and Thoracic Paravertebral Block After Uniportal Video-Assisted Thoracic Surgery: A Randomized Trial

Assiut University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2022年2月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
102
试验地点
1
主要终点
Time to first analgesic requirement

研究概览

简要总结

Although less invasive, postoperative analgesia remains challenging in patients undergoing uniportal video-assisted thoracic surgery (VATS).

详细描述

Although less invasive, postoperative analgesia remains challenging in patients undergoing uniportal video-assisted thoracic surgery (VATS).

Adequate postoperative pain relief is imperative to hasten functional recovery, accelerate discharge from the hospital, and reduce chronic postsurgical pain.

研究设计

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

入排标准

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

入选标准

  • Patients scheduled for uniportal VATS under general anesthesia, ASA status I-III, aged from 18 to 70 years old of both sex.

排除标准

  • Contraindications to regional block
  • Pregnancy
  • Body mass index (BMI) > 30 Kg/m2
  • Psychiatric diseases
  • Severe renal, liver, or cardiac dysfunction

研究组 & 干预措施

Group I

Active Comparator

Patients will receive ultrasound-guided deep serratus anterior plane block.

干预措施: Ultrasound-guided deep serratus anterior plane block with isobaric bupivacaine (Drug)

Group II

Active Comparator

Patients will receive local wound infiltration (LWI).

干预措施: Local wound infiltration with isobaric bupivacaine (Drug)

Group III

Placebo Comparator

Patients will receive ultrasound-guided thoracic paravertebral block.

干预措施: Ultrasound-guided thoracic paravertebral block with isobaric bupivacaine (Drug)

结局指标

主要结局

Time to first analgesic requirement

时间窗: 24 hours after surgery

Assessed in minutes

次要结局

  • Postoperative pain intensity(24 hours after surgery)

研究者

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

Seham Mohamed Moeen Ibrahim

Assistant professor of Anesthesia and Intensive Care

Assiut University

研究点 (1)

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