Comparing the Efficacy of Continuous and Pulsed Ultrasound Treatments in Lateral Epicondylitis

Eskisehir Osmangazi University

Status: Completed

Conditions: Lateral Epicondylitis

Treatments: Device: ultrasound

Study type: Interventional

Funder types: Other

Identifiers

NCT03944122

FTR

Details and patient eligibility

About

Objectives: The purpose of this study was to investigate the efficacy of continuous and pulsed ultrasound treatments in lateral epicondylitis and to compare the efficacy of these two treatments against each other and placebo.

Patients and Methods: Fifty one patients diagnosed with lateral epicondylitis were included to the study. Patients were randomised to continuous ultrasound, pulsed ultrasound and placebo groups by using closed envelop method. First group received continuous ultrasound treatment. Second group received pulsed ultrasound treatment in proportion as. Third group received of placebo treatment. Resting and moving pain levels of the patients were evaluated by using visual analog scale. Muscle strength was evaluated by using dynamometer. For functional evaluation Duruoz's hand index and Patient-Rated Tennis Elbow Evaluation (PRTEE) scales were used. Evaluations were made at baseline, at the end of the therapy, and one month after the therapy. In addition, at baseline and at the end of the therapy, the thickness of the common extensor tendon was measured by using ultrasonic imaging (USG).

Full description

The purpose of this study was to investigate the efficacy of continuous and pulsed ultrasound treatments in lateral epicondylitis and to compare the efficacy of these two treatments against each other and placebo.

Fifty one patients (33 women, 18 men) diagnosed with lateral epicondylitis were included to the study. Patients were randomised to continuous ultrasound (n=17), pulsed ultrasound (n=17) and placebo (n=17) groups by using closed envelop method. First group received 10 sessions of 1 W/cm2 and 1,5 MHz continuous ultrasound treatment. Second group received 10 sessions of 1 W/cm2 and 1,5 MHz pulsed ultrasound treatment in proportion as 1:4. Third group received 10 sessions of placebo treatment with the same device seemed to be working but without delivering any output. Resting and moving pain levels of the patients were evaluated by using visual analog scale. Muscle strength was evaluated by using dynamometer. For functional evaluation Duruoz's hand index and Patient-Rated Tennis Elbow Evaluation (PRTEE) scales were used. Evaluations were made at baseline, at the end of the therapy, and one month after the therapy. In addition, at baseline and at the end of the therapy, the thickness of the common extensor tendon was measured by using ultrasonic imaging (USG).

Enrollment: 51 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• aged between 18-70 years
• pain on the lateral side of the elbow for less than six months
• tenderness over the lateral epicondyle
• pain during extension of wrist and fingers

Exclusion criteria

• upper extremity and neck disorders
• other elbow pathologies
• presence of tendon rupture
• usage of non-steroidal anti inflammatory drugs
• joint limitations due to a previous radius/ulna fracture
• previous elbow surgery
• osteoporosis, malignancy, hemophilia, neurologic deficit(s) in the ipsilateral upper limb
• cognitive disfunction

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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51 participants in 3 patient groups

continuous ultrasound

Experimental group

Description:

continuous ultrasound were applied to the patients

Treatment:

Device: ultrasound

pulsed ultrasound

Experimental group

Description:

pulsed ultrasound were applied to the patients

Treatment:

Device: ultrasound

placebo

Experimental group

Description:

placebo (sham) ultrasound were applied to the patients

Treatment:

Device: ultrasound