Transcutaneous Pulse Radiofrequency Treatment for Subacromial Impingement Syndrome
Shoulder Impingement Syndrome
About this trial
This is an interventional treatment trial for Shoulder Impingement Syndrome focused on measuring Shoulder Pain, Transcutaneous radiofrequency treatment, Ultrasound
Eligibility Criteria
Inclusion Criteria:
- 18- 65 years of age
- Having (chronic) shoulder pain for more than 3 months
- No treatment for shoulder pain (physical therapy, joint area injection, radiofrequency treatment) in the past 3 months
Exclusion Criteria:
Systemic rheumatic diseases
- Malignancy, acute infections Adhesive capsulitis
- Bicipital tendinitis
- Supraspinatus tendon full-thickness rupture
- Those who have undergone surgery for shoulders and neck
- Pace maker
- Pregnant women Those with cervical radiculopathy
- Those who do not agree to participate in the study
Sites / Locations
- Gazi University Medical School, Physical Medicine and Rehabilitation Department
Arms of the Study
Arm 1
Arm 2
Sham Comparator
Active Comparator
Control Group
Study Group
In this group a pair of TCPRF electrodes will be applied to the painful shoulder at six standardized sites for 2 minutes each (approximately a total of 15 minutes). The device is not going to be activated in the control group. The device will be set at 0 V. TCPRF treatment is going to be applied for one session.
A pair of TCPRF electrodes will be applied to the painful shoulder at six standardized sites for 2 minutes each (approximately a total of 15 minutes). It will be activated in the study group. In the study group device will be set at 80 V, every pulse will continue for 10 milliseconds and 5 pulses per second. TCPRF treatment is going to be applied for one session in both groups.