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Clinical Trials in Turkey / NCT06713005
Starting soon Not applicable

The Clinical Efficacy of Different Durations of Suprascapular Nerve Pulsed Radiofrequency

NCT06713005 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-01
Last updated
2024-12-27

Condition(s) studied

Suprascapular NerveShoulder Impingement SyndromePulsed RadiofrequencyChronic PainSupraspinatus Tendinopathy

Investigational drug(s) / intervention(s)

suprascapular nerve block and 4 mins Pulsed radiofreuency application to suprascapular nervesuprascapular nerve block and 9 mins Pulsed radiofreuency application to suprascapular nerve

suprascapular nerve block and 4 mins Pulsed radiofreuency application to suprascapular nerve: suprascapular nerve pulsed rf

suprascapular nerve block and 9 mins Pulsed radiofreuency application to suprascapular nerve: suprascapular nerve block and 4 mins Pulsed radiofreuency application to suprascapular nerve

Study summary

Chronic shoulder pain due to impingement syndrome and supraspinatus tendinosis is a debilitating condition. Suprascapular nerve innervates most part of shoulder joint. Supraspinatus nerve block can be used as a part of pain therapy. However, its efficacy is short-lasting. To prolong analgesia, short bursts of electrical stimulation to suprascapular nerve may be applied. To the date there is no consensus about duration of these type of stimulation. Investigators' aim is to investigate efficacy of two different duration of stimulation (pulsed radiofrequency) on chronic shoulder pain.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18-80 years * Shoulder pain caused by impingement syndrome * Shoulder pain due to supraspinatus tendinosis * Diagnosis of impingement syndrome and supraspinatus tendinosis confirmed through physical examination and radiological imaging (MRI) * Pain persisting for 3 months or longer * Numeric Pain Rating Scale (NRS) score of 4 or higher despite conservative treatment Exclusion Criteria: * Patients unwilling to participate in the study * Presence of chronic pain due to other conditions * Presence of cervical radiculopathy * History of opioid use * Uncontrolled diabetes (HbA1c \> 8) * History of shoulder surgery on the affected side * Uncontrolled psychiatric disorders despite medical treatment * History of cancer * History of stroke

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara University Ankara Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06713005 on ClinicalTrials.gov ↗ ← All trials in Turkey