RecruitingPhase 4NCT06040112
Effect of Atelocollagen Injection in Patients With Calcific Tendinitis
Sponsor
Hyungsuk Kim
Enrollment
46 participants
Start Date
Dec 6, 2023
Study Type
INTERVENTIONAL
Conditions
Summary
Assess the clinical outcomes using atelocollagen injection in patients with calcific tendinitis.
Eligibility
Min Age: 20 YearsMax Age: 69 Years
Inclusion Criteria3
- Patients in whom calcification of 5mm or more is observed in plain radiographs.
- In cases where concomitant medication is administered continuously during the clinical trial period, patients who have verified the exact prescribed medication taken within the last week and agreed to maintain the same amount throughout the study period.
- Individuals who have agreed to participate in this study and have given written consent themselves.
Exclusion Criteria8
- Patients with a medical history of infectious arthritis, rheumatoid arthritis, tumors, or fractures.
- Patients with hypersensitivity.
- Patients with a history of anaphylactic reactions.
- Patients with ongoing autoimmune diseases or a past medical history of such diseases, either in the patient or their family members.
- Patients who are allergic to transplants. ⑥ Patients who are allergic to porcine (pig) proteins.
- ⑦ Patients deemed unsuitable for this trial based on the judgment of the trial administrator, such as those with mental illnesses.
- ⑧ Patients who have received intra-articular steroid or other injection treatments within one month prior to the procedure decision.
- ⑨ Patients who are on concomitant medications that include oral steroids.
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Interventions
DEVICEAtelocollagen
Tendoregen (Atelocollagen) injection
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06040112