Registry of Outcomes of Dezawa MuseCells®
Recruiting now
Conditions studied: Osteoarthritis (OA), Longevity, Wound Care, Pain, Orthopaedic
In brief
The goal of this observational study is to learn about the long-term effects of Dezawa MuseCells to treat various diseases. The Primary Goal: What is the short-term and long- term outcomes of Dezawa Musecells? Participants treated with Dezawa MuseCells as part of their regular medical care and will answer online survey questions about symptoms and clinical outcomes for 5 years.
Key facts
- Study ID
- NCT07645989
- Run by
- MuseCell Innovations Pte LTD
- People needed
- 5000
- Starts
- 2026-07-01
- Expected to finish
- 2031-12-31
- Last updated by the study team
- 2026-06-12
Who can join
Age: any, up to 89. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Received Dezawa MuseCells® as Part of Routine Clinical Care
- Patients ( and/or authorized representative) capable of providing informed consent and participating in long-term follow-up.
- Willingness to Complete Online Survey Assessments
- Participants must have reliable access to email or a mobile device and be willing to complete digital surveys at scheduled intervals over a 5-year period.
- Diagnosis of a Condition for Which Dezawa MuseCells® Were Administered Includes, but is not limited to, neurologic, musculoskeletal, cardiovascular, immunologic, and systemic degenerative conditions.
- Ability to Communicate in the Registry's Supported Language
- Participants must be able to read and respond to registry surveys in the designated study language.
- Enrollment Within 12 Months of MuseCell® Administration
You may not qualify if…
- Not Receive Dezawa MuseCells®-Individuals who have not been treated with Dezawa MuseCells® or received a counterfeit/non-licensed product cannot be included.
- Unable or Unwilling to Provide Informed Consent Includes individuals with cognitive impairment who lack a legally authorized representative willing to consent on their behalf.
- Inability to Participate in Long-Term Digital Follow-Up
- Concurrent Participation in an Interventional Clinical Trial Affecting Outcomes
- History of Malignancy Diagnosed Within the Past 12 Months
- Excludes patients with active or recently treated cancer unless their treating physician determines participation poses no additional safety concerns.
- Any Condition That, in the Investigator's Judgment, Would Compromise Data Quality
- Use of Non-Licensed or Counterfeit "Muse-like" Cells Ensures that registry data reflect outcomes of authentic Dezawa MuseCells® produced under licensed methods.
- Pregnant or Actively Breastfeeding at Time of Enrollment
Where it is running
- Regene Labs — Guadalajara, Mexico (enrolling)
- Bioreset Medical — North Palm Beach, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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