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临床试验/NCT06530862
NCT06530862已完成不适用

Comparison of the Efficacy of ESWT and Dry Needling Treatments in the Management of Piriformis Syndrome; A Randomized Study

Istanbul Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年2月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44
试验地点
1
主要终点
Visual analog scale (VAS) score

研究概览

简要总结

This study is being conducted on patients with piriformis syndrome. Patients are divided into two groups by list randomization method: Extracorporeal shock wave therapy (ESWT) group and Dry neddling (DN) group. Both groups of patients agreed to perform basic stretching exercises. The ESWT group received 3 sessions of radial ESWT, 1 session per week. The DN group received 3 sessions of ultrasound-guided needling, 1 session per week. Clinical evaluations of the participants were performed at the beginning of treatment, 1 month, and 3 months after treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •>18 years
  • •Complaint for more than 3 months

排除标准

  • •disc pathologies according to radiological imaging
  • •hip joint and soft tissue pathologies
  • •recent history of trauma, history of surgery in the lumbar and hip region
  • •history of rheumatologic disease
  • •history of polyneuropathy
  • •history of sciatic nerve injury
  • •history of malignancy
  • •opioid analgesia or corticosteroid intervention for pain in the last month
  • •patients receive another treatment during the study
  • •Having a contraindication for DN treatment or ESWT treatment

研究组 & 干预措施

ESWT group

Active Comparator

Patients in this group received three sessions of ESWT at an energy density of 4 bars and a frequency of 2,000 shocks/min at 5 Hz for three weeks, each session once a week.

干预措施: ESWT+stretching exercises (Other)

Dry needling

Active Comparator

The piriformis muscle of the patients in the group will be dry needled with 0.6*80 mm acupuncture needles under ultrasound guidance for 3 sessions at one week intervals.

干预措施: Dry needling+stretching exercises (Other)

结局指标

主要结局

Visual analog scale (VAS) score

时间窗: 7 months

Pain was evaluated with a Visual analog scale (VAS) score

Lower extremity functiunal scale (LEFS)

时间窗: 7 months

Pain was evaluated with a Lower extremity functiunal scale (LEFS (minimum=0, maximum=80)) The higher the score, the better the result

Oswestry disability index (ODI)

时间窗: 7 months

Pain was evaluated with a Oswestry disability index (ODI (minimum=0, maximum=60))The lower the score the better the result

次要结局

未报告次要终点

研究者

发起方
Istanbul Training and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Burak Tayyip Dede

Medical Doctor

Istanbul Training and Research Hospital

研究点 (1)

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