Lateral epicondylitis is a common musculoskeletal disorder associated with pain and impaired upper extremity function. The aim of this study was to compare the effectiveness of extracorporeal shock wave therapy (ESWT) and single-session 5% dextrose prolotherapy (DPT) in patients with lateral epicondylitis and to evaluate the relative superiority of these treatment approaches during short- and mid-to-long-term follow-up. Ninety-six patients were allocated into three groups: conventional treatment alone, conventional treatment plus ESWT, and conventional treatment plus DPT. Pain, functional status, grip strength, and common extensor tendon thickness were evaluated during follow-up.
Lateral epicondylitis is a common musculoskeletal disorder associated with pain, reduced grip strength, and impaired upper extremity function. This study aimed to compare the effectiveness of extracorporeal shock wave therapy (ESWT) and single-session 5% dextrose prolotherapy (DPT) in patients with lateral epicondylitis and to evaluate their relative effectiveness during short- and mid-to-long-term follow-up. Ninety-six patients were allocated into three groups: conventional treatment alone, conventional treatment plus ESWT, and conventional treatment plus DPT. Conventional treatment consisted of home exercise and splinting. ESWT was applied in 3 sessions (2000 pulses, 0.15 mJ/mm²), while the DPT group received a single ultrasound-guided 5% dextrose injection. Primary outcomes included Visual Analog Scale pain scores for rest, night pain, resisted wrist extension, and grip pain. Secondary outcomes included QuickDASH, PRTEE, grip strength measured with a Jamar dynamometer, and ultrasonographic assessment of common extensor tendon thickness. Clinical assessments were performed at baseline, 1, 3, and 6 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
96
Splinting and home exercise program
3 sessions, weekly, 4Hz, 2000 pulses/session, 0.15 mJ/mm².
Single-session ultrasound-guided 1 mL 5% dextrose injection.
SBU Ankara Physical Medicine and Rehabilitation Training and Research Hospital Ankara, Turkey
Ankara, Cankaya, Turkey (Türkiye)
VAS Resisted Wrist Extension Pain
Pain during resisted wrist extension assessed using the Visual Analog Scale (VAS).
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
VAS Gripping Pain
Pain intensity during gripping assessed using the Visual Analog Scale (VAS).
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
VAS Resting Pain
Resting pain assessed using the Visual Analog Scale (VAS).
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
VAS Night Pain
Night pain assessed using the Visual Analog Scale (VAS).
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
Quick-DASH Score
Functional disability assessed using the Quick Disabilities of the Arm, Shoulder and Hand questionnaire. The QuickDASH score ranges from 0 to 100, where 0 indicates no symptoms and normal upper extremity function, while 100 indicates the highest symptom severity and the poorest functional status.
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
PRTEE Score
Functional outcome assessed using the Patient-Rated Tennis Elbow Evaluation questionnaire. The PRTEE consists of 15 items divided into two subscales: pain (5 items) and function (10 items). The total score ranges from 0 to 100, with 0 indicating no pain and normal function, and 100 indicating the highest pain severity and the poorest functional status. Higher scores reflect greater pain intensity and functional impairment.
Time frame: Baseline, 1 month, 3 months, and 6 months after treatment
Grip Strength
Grip strength measured using a Jamar dynamometer.
Time frame: Baseline and 6 months
Common Extensor Tendon Thickness
Ultrasonographic measurement of common extensor tendon thickness.
Time frame: Baseline and 6 months
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