Study Stopped
company dissolved
Study to Assess the Safety and Effects of Autologous Adipose-Derived SVF Cells in Patients With Parkinson's Disease
An Open-label, Non-Randomized, Multi-Center Study to Assess the Safety and Effects of Autologous Adipose-Derived Stromal Cells Delivered Intravenously and Intranasally in Patients With Parkinson's Disease
1 other identifier
interventional
N/A
1 country
1
Brief Summary
The intent of this clinical study is to answer the questions:
- 1.Is the proposed treatment safe
- 2.Is treatment effective in improving the disease pathology of patients with Parkinson's Disease and clinical outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started May 2014
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 3, 2011
CompletedFirst Posted
Study publicly available on registry
October 18, 2011
CompletedStudy Start
First participant enrolled
May 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2017
CompletedNovember 24, 2017
November 1, 2017
3.5 years
October 3, 2011
November 21, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
UPDRS (UNIFIED PARKINSON'S DISEASE RATING SCALE)-Behavior
Improvement in Mentation, Behavior and mood in on and off position
3 months
Number of participants with adverse events
1 week
UPDRS- Improvement in Activities of Daily Living
3 months
UPDRS- Improvement in motor Examination
Values compared to baseline
3 months
UPDRS- MODIFIED HOEHN AND YAHR STAGING
Compared to baseline
3 months
UPDRS- SCHWAB AND ENGLAND ACTIVITIES OF DAILY LIVING SCALE
3 months
UPDRS (UNIFIED PARKINSON'S DISEASE RATING SCALE)Behavior
Improvement in Mentation, Behavior and mood in on and off position
6 months
Number of participants with adverse events
2 weeks
Number of participants with adverse events
4 weeks
UPDRS- Improvement in Activities of Daily Living
6 months
UPDRS- Improvement in motor Examination
6 months
UPDRS- MODIFIED HOEHN AND YAHR STAGING
6 months
UPDRS- SCHWAB AND ENGLAND ACTIVITIES OF DAILY LIVING SCALE
6 months
Secondary Outcomes (4)
Reduction of Parkinson's medications
3 months
Improvement in subjective symptoms: facial expression, gait, and freezing
3 months
Reduction of Parkinson's medications
6 months
Improvement in subjective symptoms: facial expression, gait, and freezing
6 months
Study Arms (1)
Intravenous Injection and Intanasal infusion of AD-SVF
EXPERIMENTALAD-SVF
Interventions
The adipose tissue specimen will be collected from the patient's abdomen or applicable region using a liposuction cannula. The adipose tissue is transferred to the laboratory for separation of the adipose tissue-derived stem cells, which are then transferred for catheter injection.
Eligibility Criteria
You may qualify if:
- Males and Females between Age 18 and 80 years.
- Patient with current diagnosis of PD with motor complications (as confirmed by neurologist) as per the standard criteria and guidelines.
- Responsiveness to Levodopa or dopa agonist. This is defined as improvement between Off and On UPDRS by at least 33% of the Motor UPDRS.
- PD of Stage 2.5, 3 \& 4 of HOEHN \& YAHR staging.
- Stable Parkinsonian medications for the 60 days prior to the surgical therapy.
- MRI not showing gross atrophy or any other pathology of brain.
- Patients with score less than 19 for the Montgomery-Asberg Rating Scale (MADRS) for Depression.
- NO Significant cognitive impairment.MMSE \> 21.
- Up to date on all age and gender appropriate cancer screening per American Cancer Society
You may not qualify if:
- History of intracranial surgeries or implantation of a device for Parkinson's disease two years prior to treatment.
- History of psychiatric disorders like schizophrenia or psychotic disorders.
- History of other malignancy, with the exception of treated cutaneous squamous cell or basal cell carcinoma, within 5 years.
- Contraindication for MRI
- Females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study
- Life expectancy \< 6 months due to concomitant illnesses.
- Exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study.
- Active infectious disease. Patients known to have tested positive for HIV, HTLV, HBV, HCV, CMV (IgM \> IgG) and/or syphilis will be evaluated by an expert as to patient eligibility based on the patient's infectious status
- Any illness which, in the Investigator's judgement, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results
- Patients on chronic immunosuppressive transplant therapy
- Systolic blood pressure (supine) ≤90 mmHg;
- Resting heart rate \> 100 bpm;
- Active clinical infection being treated by antibiotics within one week of enrollment.
- Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate.
- History of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last two years.
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ageless Regenerative Institute LLC
Aventura, Florida, 33180, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sharon McQuillan, MD
Ageless Regenerative Institute
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 3, 2011
First Posted
October 18, 2011
Study Start
May 1, 2014
Primary Completion
November 1, 2017
Study Completion
December 1, 2017
Last Updated
November 24, 2017
Record last verified: 2017-11