IRCT20220506054756N1招募中未知
Comparison of Acupuncture and High Intensity Laser Therapy on Pain, Quality of Life and Disability of Patients with Disc Herniation in Patients with Chronic Low Back Pain, a Randomized Control Study
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 60
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
- 18 years 至 60 years（—）
- 性别
- All
入选标准
- •Patients aged 18 to 60 years
- •They signed informed consent forms and volunteered to participate in the experiments
- •They have had back pain for more than 3 months On examination
- •they have local sensitivity in the back, buttocks and legs, and shooting pain, and they have a Straight Leg Rising (SLR) test or a Slump test
- •MRI of the lumbar disc herniation was seen
- •Have the mental ability to answer questionnaire questions
排除标准
- •Acute trauma or fracture of the lumbar spine or dysplasia of the spinal structure (spondylolysis)
- •Congenital anomaly, abdominal aneurysm 3. Lumbar spine surgery Uncontrolled or severe metabolic disorders or cardiovascular, hepatic and renal disorders
- •Lumbar spine surgery
- •Uncontrolled or severe metabolic disorders or cardiovascular, hepatic and renal disorders
- •Inflammatory pain
- •Severe or progressive neurological disorders or lumbar instability
- •Physiotherapy treatments on the back in the last 3 months
- •History of lumbar injection in the last 4 weeks
- •Severe osteopenia
- •Systemic rheumatic disease (rheumatoid arthritis and fibromyalgia)
- •Spinal cancers and patients with spinal tuberculosis
- •Danger symptoms include nocturnal pain, recent involuntary weight loss, and symptoms of Cauda equina syndrome
- •Spondylolisthesis
- •Hypersensitivity to piroxicam and methocarbamol
- •Patients who have undergone lumbar spine fusion or have indication for surgery
- •Pregnant patients
- •Patients who have had a tattoo or melanocytic moles in or near the treatment areas
- •Patients with lupus or any other autoimmune disease, thrombophlebitis or anemia, and skin allergies
- •Not participating in treatment sessions for more than 2 sessions
- •Dissatisfaction with participating in the study at any stage of the study
- •No referral for follow-up 4 weeks later and no phone response 3 months after starting treatment
- •Emergence of severe medical diseases during the study that affect the individual's referral and follow-up
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