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Pain Managment in Chronic Shoulder Pain

Unknown statusNot applicableNCT06106490
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The purpose of this study is to evaluate the effect of adding pulsed radiofrequency (PRF) modality to suprascapular nerve injection with ultrasound glenohumeral steroid in chronic shoulder pain patients focusing on both changes in pain and function scores

Study details

Official title
Addition of Pulsed Radiofrequency to Suprascapular Nerve Block With Glenohumeral Steroid Injection in Patients With Chronic Shoulder Pain
Conditions
  • Chronic Pain Management
Interventions
  • Other: the effect of adding pulsed radiofrequency (PRF) modality to suprascapular nerve injection with ultrasound glenohumeral steroid in chronic shoulder pain patients
Sponsor
Ain Shams University
Start date
2023-11-01
Primary completion
2024-10-30
Sex
All
Age range
from 21 Years to 60 Years
Results posted
No results posted in this snapshot
Countries
Egypt
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adults aged from 21-60 years. * Patients with American Society of Anesthesiologists (ASA) physical status I and II. * Chronic shoulder pain (\>3 months) and will undergo interventional treatment due to inadequate response to conservative treatments. Exclusion Criteria: * Refusal of procedure or participation in the study by patients. * History of shoulder surgery, another intervention history between 3 months before and 1 year after the intervention applied. * Patients with chronic pain syndrome due to other shoulder pathology (fibromyalgia, cervical discopathy, brachial plexus injury). * Uncontrolled diabetes mellitus patients with glycated hemoglobin (HbA1C) levels of more than 7%. * Patients with known history of allergy to the study drugs. * Infection at site of injection. * Cognitive or psychiatric illness that will lead to inability to cooperate, speak, or provide informed consent.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06106490