Effect of Percutaneous Electrolysis Combined With Exercise on Pain and Function in Chronic Lateral Epicondylitis: A Randomized Controlled Trial
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
- 否
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
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
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
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
Serkan Polat
MD
Sivas State Hospital
