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Clinical Trials/KCT0007820
KCT0007820
Recruiting
未知

Validity of intravenous indocyanine green injection as a diagnostic tool for soft tissue assessment in shoulder and elbow arthroscopic surgery

Asan Medical Center0 sites110 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Asan Medical Center
Enrollment
110
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) Patients with chronic or recurrent lateral epicondylitis of the main node corresponding to indications for surgery
  • 2\) Patients with rupture of the rotator cuff of the shoulder joint corresponding to surgical treatment indications
  • 3\) Patients with systemic diseases who do not have a reason for disqualification from surgery and contrast agent injection
  • 4\) Patients who are willing to voluntarily agree in writing after receiving an explanation of the purpose, method, etc. of this study, comply with the test plan, and are willing to visit the hospital for the evaluation of observation items.

Exclusion Criteria

  • 1\) Patients with inflammatory or rheumatoid arthritis
  • 2\) Patients with joint stiffness due to deformation of the humerus, radial bone, and ulnar bone that make up the main section
  • 3\) Patients with advanced arthritis who are indications for joint replacement
  • 4\) Patients with observed soft tissue lesions other than lateral epicondylitis
  • 5\) Patients with soft tissue lesions other than shoulder joint rotator cuff rupture observed
  • 6\) Those who have been diagnosed with the following diseases and find it difficult to proceed with the operation
  • A. Uncontrolled diabetes, high blood pressure
  • B. Severe mental illness
  • c. Severe cirrhosis, renal failure, heart failure
  • 7\) Those who are deemed inappropriate for clinical trials by the investigator responsible for the trial or other researchers

Outcomes

Primary Outcomes

Not specified

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