Skip to main content
Clinical Trials/NCT05015322
NCT05015322
Completed
Phase 4

Comparison of the Effectiveness of the Ultrasound Guided Subacromial, Acromioclavicular With Subacromial Injection and Suprascapular Nerve Block in Patients With Shoulder Impingement Syndrome ; A Randomized Controlled, Single Blind, Clinical Trial

Bursa Yüksek İhtisas Education and Research Hospital0 sites88 target enrollmentJanuary 1, 2017

Overview

Phase
Phase 4
Intervention
bupivacaine and methylprednisolone
Conditions
Shoulder Impingement
Sponsor
Bursa Yüksek İhtisas Education and Research Hospital
Enrollment
88
Primary Endpoint
Visual Analogue Scale (VAS)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Shoulder pain, which is the third most common cause of musculoskeletal pain, has different etiologies. Muscle, bone structures and connective tissue pathologies can cause shoulder pain. Impingement syndrome (IS), which can cover many terms such as rotator cuff disorders, tendinitis and tears, is one of the most common pathologies of shoulder pain.

Detailed Description

The hypothesis of this study was that injection types including ACJ would increase treatment efficacy.Therefore, this study investigated the six-month follow-up results of patients undergoing SA injection and SSNB and those receiving SA and ACJ injection.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
January 1, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bursa Yüksek İhtisas Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr. Burcu Metin Ökmen

Principal Investigator,Assoc.Phd.M.D.

Bursa Yüksek İhtisas Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • patients aged 18-65,
  • who were suffering from shoulder pain for more than three months and
  • who were diagnosed with IS.
  • All patients included in the study were diagnosed with IS using Shoulder Magnetic Resonance imaging.

Exclusion Criteria

  • the presence of cervical radiculopathy;
  • undergoing shoulder operation before;
  • the presence of central nervous system or
  • the presence of rheumatological disease, and polyneuropathy;
  • receiving physical therapy in the shoulder area with a diagnosis of IS within the last six months; and
  • receiving any injection therapy in the past.

Arms & Interventions

subacromial injection

ultrasound (US)-guided subacromial injection

Intervention: bupivacaine and methylprednisolone

acromioclavicular joint and subacromial injection

ultrasound (US)-guided acromioclavicular joint and subacromial injection

Intervention: bupivacaine and methylprednisolone

suprascapular nerve block

ultrasound (US)-guided suprascapular nerve block

Intervention: bupivacaine and methylprednisolone

Outcomes

Primary Outcomes

Visual Analogue Scale (VAS)

Time Frame: six month

for pain. 0: no pain at all, 10: worst pain imaginable

Secondary Outcomes

  • Shoulder pain and disability index (SPADI)(six month)
  • Short-Form 12 (SF-12)(six month)

Similar Trials