Ultrasound-Guided Suprascapular Pulsed Radiofrequency

PAIN, INTRACTABLE, Shoulder Clinical Trial

— PRF  

Official title:

Effects of Ultrasound-Guided Suprascapular Pulsed Radiofrequency Therapy on Chronic Shoulder Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03251703
• Other study ID #: Sakaray University
• Status: Completed
• Phase: N/A
• First received: August 13, 2017
• Last updated: August 15, 2017
• Start date: January 1, 2015
• Est. completion date: March 1, 2017

Study information

• Verified date: August 2017
• Source: Sakarya University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Shoulder pain is the second most common musculoskeletal disease in adults, and it often becomes chronic due to treatment difficulties.

Pulsed radiofrequency (PRF) therapy has become increasingly popular in the treatment of chronic shoulder pain due to its long duration of action and non-destructive method.

Description:

These patients lacked pain control despite systemic analgesics and conservative therapy and applied to our pain polyclinics for shoulder pain lasting at least 3 months.

The ultrasound-guided SSPRF was performed in those patients with a reduction of 50% or more VAS score and those that reported healing in the AROM in the diagnostic SNB.

The resting, motion and sleeping shoulder pain assessments of the patients were done using a visual analog scale (VAS). The shoulder joint function was assessed using the Shoulder Pain and Disability Index (SPADI) questionnaire and the active range of motion (AROM) of the joint was measured using a goniometer In this study, investigators aimed to reveal the effects of ultrasound-guided suprascapular PRF (SSPRF) therapy applied to patients with chronic shoulder pain on both shoulder pain and function.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 74
• Est. completion date: March 1, 2017
• Est. primary completion date: January 1, 2016
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Patients 18 years of age or older who were diagnosed with at least one of the following:

adhesive capsulitis of the shoulder (M75.0), rotator cuff syndrome (M75.1), and impingement syndrome of shoulder (M75.4) according to the ICD-10 classifications. These patients lacked pain control despite systemic analgesics and conservative therapy (like physiotherapy) and applied to our pain polyclinics for shoulder pain lasting at least 3 months.

Exclusion Criteria:

Patients with other diseases causing chronic pain, those with neuropathic pain, those who had undergone surgery on the same shoulder, those with an allergy history from local anesthesia, those with abnormal coagulation tests, and those with cardiac pacemakers were excluded from this study.

Related Conditions & MeSH terms

• Pain, Intractable
• PAIN, INTRACTABLE, Shoulder

Intervention

Procedure:
• Ultrasound-Guided Suprascapular Pulsed Radiofrequency .
The ultrasound-Guided Suprascapular Pulsed Radiofrequency was administered under operating room conditions while the patient was monitored in a sitting position.An ultrasound-guided 22 G 5-mm active-tip 100-mm radiofrequency needle (SC-K; Top Neuropole, Tokyo, Japan) was pushed forward towards the suprascapular notch until it passed the transverse scapular ligament using an in-plane approach.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Sakarya University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluation of The Efficacy of Ultrasound-Guided Suprascapular Pulsed Radiofrequency	Retroscopic study	1 years