NCT07645989 · MuseCell Innovations Pte LTD
Registry of Outcomes of Dezawa MuseCells®
What this study is about
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.
View original scientific description
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.
Interventions
OTHER
MuseCell Treatment
Patients undergoing treatment with Dezawa MuseCells
Primary outcome measures
Change in Patient Reported Symptom Severity
Time frame: Baseline; 1 month; 3 months; 6 months; 12 months; annually through 5 years.
Change in condition-specific symptom severity following Dezawa MuseCell® administration.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- 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
Exclusion criteria
- 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
- North Palm Beach, Florida
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Jun 12, 2026 · Source of record for eligibility and locations