跳至主要内容
临床试验/NCT07277127
NCT07277127已完成不适用

Effect of Percutaneous Electrolysis Combined With Exercise on Pain and Function in Chronic Lateral Epicondylitis: A Randomized Controlled Trial

Sivas State Hospital1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2025年9月5日最近更新:
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
68
试验地点
1
主要终点
Change in Pain Intensity (VAS)

研究概览

简要总结

The aim of this randomized controlled trial is to compare the effects of percutaneous electrolysis combined with exercise versus exercise alone on pain and function in patients with chronic lateral epicondylitis. Participants will be randomly allocated into two parallel groups. The control group will receive a 2-week exercise program including stretching and eccentric strengthening exercises for the wrist extensor and forearm muscles. The experimental group will receive the same exercise program plus three sessions of ultrasound-guided percutaneous electrolysis applied to the extensor carpi radialis brevis tendon insertion at the lateral epicondyle (on days 1, 8, and 14). Clinical outcomes will be assessed using a 10-cm Visual Analog Scale (VAS) for pain intensity, pressure pain threshold over the common extensor tendon measured with a handheld algometer, the Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire for pain and functional disability, and the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) questionnaire for upper limb function. Assessments will be performed at baseline, and then at 1 week, 1 month, and 3 months after the end of the 2-week treatment period. The study aims to determine whether adding percutaneous electrolysis to an exercise program provides greater improvement in pain and functional status than exercise alone in patients with chronic lateral epicondylitis.

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
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years
  • Clinically and MRI-confirmed diagnosis of chronic lateral epicondylitis (symptoms ≥ 3 months)
  • Ability and willingness to comply with the treatment protocol and follow-up schedule

排除标准

  • Previous elbow surgery or fracture in the affected limb
  • Local corticosteroid injection or other invasive treatment in the past 3 months
  • Cervical radiculopathy, systemic rheumatic disease, or other neurological disorders affecting the upper limb
  • Presence of a cardiac pacemaker or diagnosis of epilepsy
  • Pregnancy or breastfeeding
  • Serious bleeding disorder (coagulopathy) or current anticoagulant therapy
  • Inability to follow the exercise protocol or attend follow-up visits

研究组 & 干预措施

Exercise

Active Comparator

Participants perform a 2-week exercise program including stretching and eccentric strengthening exercises for the wrist extensor and forearm muscles.

干预措施: Exercise (Other)

Percutaneous Electrolysis plus Exercise

Experimental

Participants receive the same 2-week exercise program as the control group plus three sessions of ultrasound-guided percutaneous electrolysis applied to the extensor carpi radialis brevis tendon insertion at the lateral epicondyle on days 1, 8, and 14.

干预措施: Exercise (Other)

Percutaneous Electrolysis plus Exercise

Experimental

Participants receive the same 2-week exercise program as the control group plus three sessions of ultrasound-guided percutaneous electrolysis applied to the extensor carpi radialis brevis tendon insertion at the lateral epicondyle on days 1, 8, and 14.

干预措施: Percutaneous Electrolysis (Device)

结局指标

主要结局

Change in Pain Intensity (VAS)

时间窗: Baseline, 1 week post-treatment, 1 month, 3 months

Pain intensity will be measured using a 10-cm Visual Analog Scale (VAS).

次要结局

  • Change in Pressure Pain Threshold (Algometry)(Baseline, 1 week post-treatment, 1 month, 3 months)
  • Change in Functional Status (PRTEE Score)(Baseline, 1 week post-treatment, 1 month, 3 months)
  • Change in Upper Limb Function (QuickDASH)(Baseline, 1 week post-treatment, 1 month, 3 months)

研究者

发起方
Sivas State Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Serkan Polat

MD

Sivas State Hospital

研究点 (1)

Loading locations...

相似试验