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Clinical Trials/NCT04461522
NCT04461522
Unknown
Not Applicable

Prospective Cohort Study on the Outcome of Treatment of Rotator Cuff Injury by Ultrasound-guided

Peking University Third Hospital1 site in 1 country134 target enrollmentMarch 10, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rotator Cuff Injury
Sponsor
Peking University Third Hospital
Enrollment
134
Locations
1
Primary Endpoint
Shoulder function
Last Updated
5 years ago

Overview

Brief Summary

Rotator cuff injury is a common shoulder joint disease in clinic. If conservative treatment fails to improve pain symptoms and range of motion, the surgical indications are. Numerous studies have shown that the pain of rotator cuff injury usually comes not from the broken tendon, but from periarthritis tendonitis, bursitis or adhesive shoulder capsule, etc. Ultrasound-guided drug injection combined with conventional rehabilitation treatment can significantly improve the pain symptoms and increase joint mobility. This study intends to use prospective cohort study methods, exposed factors for ultrasound-guided injection drug treatment, establish a rotator cuff injury exposure group and the control group of shoulder joint dysfunction queue, whether of ultrasound guided drug injection therapy can increase the shoulder joint function analysis, and explore for the rotator cuff injury method provides the basis of the evidence-based conservative treatment. The establishment of a conservative treatment cohort for rotator cuff injury will also lay the foundation for the accurate rehabilitation treatment of rotator cuff injury.

Registry
clinicaltrials.gov
Start Date
March 10, 2020
End Date
December 31, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Chief complaint around shoulder joint discomfort or restricted movement
  • Nuclear magnetic or ultrasound in the diagnosis of rotator cuff injury and not to consider surgery patients
  • Assessed by the musculoskeletal ultrasound images, diagnosed with tendonitis around shoulder joint, slippery bursa phlogistic or adhesive shoulder level
  • Section capsule, such as indications of patients treated with ultrasound guided by injection.

Exclusion Criteria

  • History of shoulder fractures, open trauma, or surgery combined with shoulder and hand syndrome, gout, autoimmune arthritis, infectious arthritis, and other factors resulting in shoulder pain or limited mobility

Outcomes

Primary Outcomes

Shoulder function

Time Frame: 6 months

Constant Test

Study Sites (1)

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