跳至主要内容
临床试验/KCT0009454
KCT0009454尚未招募Unknown

Feasibility, Safety, and Effectiveness of Ultrasound-guided Acupotomy Treatment for Degenerative Cervical Radiculopathy: a pilot randomized controlled trial

Pusan National University Korean Medicine Hospital0 个研究点目标入组 32 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
32

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
30(Year) 至 75(Year)(—)
性别
All

入选标准

  • 1) aged 30 years and older but younger than 75 years
  • 2) pain or discomfort (numbness, paresthesia, muscle weakness) in the cervical spine and upper extremities = VAS 30mm
  • 3) Symptom duration of 3 months or more
  • 4) confirmed to have intervertebral disc herniation, stenosis, or spondylosis on imaging examination (CT or MRI)
  • 5) Individuals who have received a final diagnosis of degenerative cervical radiculopathy based on comprehensive physical examination, medical history, and imaging examination results
  • 6) Individuals who voluntarily decide to participate after being informed of the study purpose and procedure and provide written informed consent

排除标准

  • 1) History or current signs of myelopathy
  • 2) Other spinal diseases or other medical conditions (e.g., thoracic outlet syndrome, carpal tunnel syndrome, plexopathy) that could cause similar symptoms to radiculopathy
  • 3) History of cervical spine surgery or planned surgery during the study period
  • 4) Serious medical history of cervical spine fracture, luxation, tumor, congenital abnormality
  • 5) Infectious or non-infectious spondylitis (e.g., ankylosing spondylitis, rheumatoid arthritis)
  • 6) Individuals taking anticoagulants or antiplatelet drugs, or with bleeding disorders that may affect hemostasis
  • 7) History of receiving epidural injections, nerve blocks, or other injections within 2 months
  • 8) Individuals with acupuncture hypersensitivity, metal allergies, severe atopic dermatitis, keloid skin, or other skin hypersensitivity
  • 9) Individuals with significant neuropsychiatric medical history or current illness
  • 10) Individuals with a history of alcoholism or drug abuse
  • 11) Pregnant or lactating women or those planning to become pregnant
  • 12) Individuals who are unable to self-report consent/data or require assistance from a caregiver/researcher to do so
  • 13) Other individuals deemed inappropriate by the clinical research coordinator

研究者

发起方
Pusan National University Korean Medicine Hospital

相似试验

尚未招募
Unknown
ltrasound-guided Acupotomy Treatment for Degenerative Lumbar Spinal Stenosis
KCT0009324Pusan National University Korean Medicine Hospital50
进行中(未招募)
不适用
Evaluating the efficacy, safety, tolerability of use and treatment adherence in two different dosing schedules, pre-costagionale and costagionale, of a sublingual allergoid (Lais Parietaria)administered to patients suffered from oculorhinitis with or without bronchial asthma by Parietaria. Randomized double-blind, multicenter, parallel group, placebo-controlled. - ParLais/09Subjects with Parietaria pollen allergy.MedDRA version: 9.1Level: LLTClassification code 10039776Term: Seasonal allergic rhinitis
EUCTR2008-007657-12-ITOFARMA
终止
不适用
Investigating the effect of supported motivational interviewing on physical activity for people with knee osteoarthritis who have already completed a widespread exercise-therapy program (GLA:D®). A pilot study.Musculoskeletal - OsteoarthritisPhysical Medicine / Rehabilitation - PhysiotherapyPublic Health - Health promotion/educationKnee Osteoarthritis
ACTRN12621000267853Miss Emily Bell32
尚未招募
不适用
Feasibility, Safety and Clinical outcomes with a new design of artificial lens fixated to capsule of lens implanted after extraction of lens opacity/cataract
CTRI/2019/02/017387ethradhama Superspeciality Eye Hospital
招募中
3 期
ltrasound-Assisted Neuraxial Anaesthesia for Caesarean SectioDifficult neuraxial anaesthesia for elective Caesarean sectionAnaesthesiology - AnaestheticsReproductive Health and Childbirth - Childbirth and postnatal care
ACTRN12614000076673Queensland Health216