Long-Term Follow-up Study to Evaluate Long-Term Safety and Efficacy of Allogenic Umbilical Cord-derived Mesenchymal Stem Cell in Patients With Rotator Cuff Disease
Recruiting now
Conditions studied: Rotator Cuff Disease
In brief
The purpose of this study is to evaluate Long-Term Safety and Efficacy of Allogenic Umbilical Cord-derived Mesenchymal Stem Cell in Patients with Rotator Cuff Disease
Key facts
- Study ID
- NCT07374679
- Run by
- Seoul National University Hospital
- People needed
- 21
- Starts
- 2026-01-27
- Expected to finish
- 2032-01-30
- Last updated by the study team
- 2026-05-22
Who can join
Age: 19 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects who received the investigational medicinal product in the Phase 1/2a clinical trial (ASB-IP-001).
- Subjects who voluntarily agreed to participate in this long-term follow-up study and provided written informed consent.
You may not qualify if…
- Subjects who cannot be contacted by any means, including telephone, mail, or e-mail, and for whom follow-up assessment is therefore not feasible.
- Subjects deemed inappropriate for participation in this long-term follow-up study at the investigator's discretion, including:
- Cases in which participation in the study may pose a significant risk to the subject's health or safety; ② Cases in which long-term follow-up visits or assessments are practically impossible due to cognitive impairment, communication difficulties, or similar conditions; ③ Cases in which continued participation in follow-up is unlikely due to difficulty adhering to the study schedule (e.g., prolonged hospitalization, long-term residence abroad).
Where it is running
- Joint & Spine Center, SMG-SNU Boramae Medical Center, Department of Orthopedic Surgery, Seoul National University College of Medicine — Seoul, Korea, South Korea (enrolling)
Full record on ClinicalTrials.gov
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