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临床试验/NCT05586633
NCT05586633Unknown不适用

The Efficacy of Ultrasound-guided Deep Paravertebral-periforaminal Ozone Injection in the Treatment of Patients With Chronic Low Back Pain

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital2 个研究点 分布在 2 个国家目标入组 50 人开始时间: 2021年11月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
50
试验地点
2
主要终点
Oswestry Disability Index (ODI)

研究概览

简要总结

Low back pain is a common disorder that every individual in the society is likely to meet throughout his/her life. Low back pain lasting longer than 12 weeks is defined as chronic low back pain and causes serious disability in the community. Conservative, pharmacological, interventional and surgical treatment options are available in its treatment. In this study, it was aimed to determine the effects of ultrasound-guided deep paravertebral periforaminal ozone injection treatment on physical examination, functional independence, quality of life and pain scores in patients with chronic low back and leg pain and to compare it with transforaminal epidural steroid injection treatment.

详细描述

A total of 50 patients were included in the study. Deep paravertebral periforaminal ozone injection was administered to the patients in the ozone injection group 4 times under ultrasound guidance, 10 ug/ml 5ml twice a week in the first week and 15 ug/ml 5ml twice a week in the second week. In the transforaminal epidural steroid injection group, steroid (dexamethasone 8mg/2ml 2ml) injection was performed under the guidance of fluoroscopy. The patients in both groups were offered a home exercise program for therapeutic waist and abdominal muscles to do during the treatment follow-up period. Patients' quality of life was evaluated with SF-36(Short Form-36), pain scores with VAS(Visüel Analog Scala) and functional evaluations with ODI(Oswestry Disability Index) at 15 days, 1 month, and 2 months. Physical examination findings were evaluated before starting the treatment and at the 2nd month follow-up.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Back and leg pain lasting longer than 3 months
  • Diagnosis of lumbar disc herniation with advanced imaging techniques after anamnesis, - physical examination and laboratory examinations
  • Continuation of complaints despite conservative treatment before
  • Regular participation in the study voluntarily

排除标准

  • Being pregnant and breastfeeding
  • History of lomber surgery
  • Peripheral neuropathy (diabetes, alcoholism...)
  • Cauda equina syndrome or progressive neurologic deficit in the lower extremity
  • Neurogenic bladder/bowel syndrome
  • Arterial vascular disease-Vascular claudication
  • Spinal stenosis, spondylolysis, spondylolisthesis
  • Local infection at the injection site
  • Presence of bleeding diathesis
  • Neuro-degenerative diseases
  • Uncontrolled diabetes, hypertension
  • History of malignancy
  • Uncontrolled psychiatric illness
  • BMI over 40
  • Allergy to injection substances

结局指标

主要结局

Oswestry Disability Index (ODI)

时间窗: 2nd week, 4th week, 8th week pain change

In the ODI questionnaire, the effect of low back pain on activities of daily living is questioned. In the test, which consists of 10 questions in total, the patient's pain intensity, the effects of pain on personal care, walking, lifting weights, standing, sitting, sleeping, sexual life, social life and traveling are questioned. The patient can get a minimum of 0 and a maximum of 5 points from each question. The maximum score to be taken from the test is 50. The patient's score is found by dividing the total score of the patient by 50, which is the maximum score, and calculating the percentage. (Patient's score ÷ maximum score × 100). Accordingly, it is calculated how much the patient's life activities are affected.

Physical examination-femoral nerve stretch test

时间窗: 2nd week, 4th week, 8th week examination change

femoral nerve stretch test - It is recorded whether there is normal or abnormal

Physical examination-straight leg raise test

时间窗: 2nd week, 4th week, 8th week examination change

straight leg raise test- It is recorded whether there is normal or abnormal

Quality of life - Short Form-36 (SF-36)

时间窗: 2nd week, 4th week, 8th week quality of life change

Satisfaction assessed by the SF-36. Short Form (SF-36) was used to investigate the quality of life of the patients.The reliability and validity of the Turkish version of SF-36 has been demonstrated. SF-36 consists of 36 questions on eight different subscales including physical functioning, role limitations due to physical health problems, bodily pain, general health perceptions, energy and fatigue, vitality, social functioning, role limitations due to emotional problems and general mental health. Each subscale of SF-36 is scored between 0 and 100, and higher scores show better Quality of life.

Physical examination-Lumbar joint range of motion examination

时间窗: 2nd week, 4th week, 8th week examination change

Lumbar joint range of motion examination( flexion-extansion-lateral flexion-rotation)

Physical examination-Walleix palpation

时间窗: 2nd week, 4th week, 8th week examination change

Walleix palpation- It is recorded whether there is tenderness in Walleix palpation.

PAİN-Visual Analog Scala (VAS)

时间窗: 2nd week, 4th week, 8th week pain change

Visual Analog Scala (VAS), patients are asked to circle the number between 0 and 10 that fits best to their pain intensity. Severity of pain was assessed VAS using the standard 10 cm (back pain and leg pain) with 0 meant "no pain" at one end, and 10 meant "unbearable pain" at the other end.

次要结局

未报告次要终点

研究者

发起方
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sefa Gümrük Aslan

Principal Investigator

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

研究点 (2)

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