The comparison study of effectiveness of dry needling and ultrasound-guided interfascial hydrodissection at upper trapezius muscle in myofascial pain syndrome: A randomized controlled trial

Sirindhorn National Medical Rehabilitation Institute0 个研究点目标入组 36 人开始时间: 2021年5月18日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

•1. Age 18 to 70 years old
•2. Be diagnosed by the physiatrist as Myofascial pain syndrome at upper trapezius muscle followed by Simon's criteria
•3. Duration of pain from 2 weeks to 3 months with VAS at least 4
•4. Have active trigger point at least 1 point at upper trapezius muscle
•5. Understand Thai language, able to read and write the questionnaire, able to follow whole process of the trial

•1.History and physical examination compatible with cervical radiculopathy or myelopathy
•2.Rheumatologic disease such as rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus
•3.History of surgery at cervical region
•4. History of trauma at cervical region
•5. Experience the treatment: dry needling, Interfascial hydrodissection, local injection, physical modalities and other physiotherapy session at shoulder and upper back region within 4 weeks before recruitment
•6.Allergy to Paracetamol and NSAIDs in the Proprionic acid subgroup such as Naproxen, Ibuprofen
•7.Pregnancy
•8.Participants who request physiotherapy session, other medications, which are not Paracetamol and Naproxen, or other treatments at upper trapezius at shoulder and upper back region during the study

发起方

Sirindhorn National Medical Rehabilitation Institute