None listed
Conditions
Interventions
Procedure/Surgery : Transcatheter embolization is performed. Transcatheter embolization is performed by approaching the radial artery and performing angiography on the painful area. After confirming a
Sponsors
Chung-Ang Univerisity Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ? Patients who have voluntarily signed a written informed consent form after receiving an explanation of the purpose, methods, and potential effects of the clinical trial ? Patients aged between 19 and 85 years ? Patients with pain persisting for more than 3 months in the affected area and with a history of receiving physical therapy, analgesics/anti-inflammatory medications, or local injection treatments ? Patients with a measured shoulder joint range of motion (ROM) of less than 90 degrees ? Patients who agree not to receive any conservative treatment other than those permitted in this clinical trial (physical therapy, medication [NSAIDs, opioid analgesics, acetaminophen], intra-articular injections such as hyaluronic acid) ? Patients who are willing to comply with the treatment and procedures of the clinical trial and participate in all follow-up evaluations through hospital visits or telephone surveys
Exclusion criteria
Exclusion criteria: ? Patients with a history of surgery on the shoulder joint targeted for the clinical trial prior to screening ? Patients suspected of having a full-thickness rotator cuff tear ? Patients with bleeding disorders or coagulopathies (e.g., idiopathic thrombocytopenic purpura, hemophilia, disseminated intravascular coagulation) ? Patients with advanced atherosclerosis or vasospasm in the arm vessels, or those expected to have such conditions ? Patients with a known hypersensitivity to gelatin ? Patients with a known hypersensitivity to contrast media ? Patients who are pregnant or breastfeeding ? Patients with a localized infection at the pain site ? Patients deemed inappropriate for participation by the investigator due to ethical concerns or potential impact on the clinical trial results
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS(Visual Analog Scale) score | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual Analog Scale (VAS) scores at early follow-up;Shoulder joint range of motion (ROM);American Shoulder and Elbow Surgeons (ASES) score;Single Assessment Numeric Evaluation (SANE) score;Patient satisfaction with treatment;Structural changes of the shoulder joint assessed by magnetic resonance imaging (MRI) | — |
Countries
Korea, Republic of
Contacts
Public ContactWoosun Choi
Chung-Ang Univerisity Hospital
Outcome results
None listed