NCT01453803

Brief Summary

The intent of this clinical study is to answer the questions:

  1. 1.Is the proposed treatment safe
  2. 2.Is treatment effective in improving the disease pathology of patients with Parkinson's Disease and clinical outcomes.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started May 2014

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
withdrawn

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

Completed
15 days until next milestone

First Posted

Study publicly available on registry

October 18, 2011

Completed
2.5 years until next milestone

Study Start

First participant enrolled

May 1, 2014

Completed
3.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2017

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

November 24, 2017

Status Verified

November 1, 2017

Enrollment Period

3.5 years

First QC Date

October 3, 2011

Last Update Submit

November 21, 2017

Conditions

Keywords

LiposuctionADSCASCstem cellParkinson's DiseaseParkinson'stherapy

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

EXPERIMENTAL

AD-SVF

Procedure: Harvesting and Implantation of Adipose-Derived Stem Cells

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.

Intravenous Injection and Intanasal infusion of AD-SVF

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Parkinson Disease

Condition Hierarchy (Ancestors)

Parkinsonian DisordersBasal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMovement DisordersSynucleinopathiesNeurodegenerative Diseases

Study Officials

  • Sharon McQuillan, MD

    Ageless Regenerative Institute

    PRINCIPAL INVESTIGATOR
0

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

Locations