跳至主要内容
临床试验/JPRN-UMIN000049105
JPRN-UMIN000049105已完成Unknown

Effect of portable ultrasound-guided trigger point block with levobupivacaine on myofascial pain syndrome in patients with advanced cancer - Effect of portable ultrasound-guided trigger point block on myofascial pain syndrome in patients with advanced cancer

Shinshu University0 个研究点目标入组 39 人开始时间: 2022年10月5日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
39

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 85years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Subjects taking anticoagulants or antiplatelet drugs (2) Subjects who are suggested to be prone to bleeding (3) Subjects with severe cytopenia (4) Those who are suggested to be susceptible to infection (5) Subjects with skin abnormalities such as redness, swelling, and edema at painful areas suspected of MPS (6) Subjects with chronic heart failure (7) Subjects with serious renal impairment (8) Subjects with severe liver disorder (9) Subjects who are allergic to local anesthetics (10) Subjects whose cause of the pain may be other than MPS due to bed rest (11) Body Mass Index (BMI) of 35 or more, or those who have difficulty in visualizing the muscle layer of the MPS pain site with a portable ultrasound device (12) Subjects who cannot keep quiet during the procedure (13) A person judged to have no decision-making capacity (14) Others who are judged to be inappropriate as subjects by the principal investigator

研究者

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