- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00766948
The Parkinson's Disease NeuroGenebank at Scripps Clinic Registry
January 15, 2025 updated by: Eric Topol, MD, Scripps Translational Science Institute
By creating a neurogenebank from Parkinson's disease patients' blood donations we will ultimately be able to define genes for Parkinson's disease and other neurological conditions.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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California
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La Jolla, California, United States, 92037
- Scripps Translational Science Institute
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La Jolla, California, United States, 92037
- The Scripps Research Institute
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La Jolla, California, United States, 92037
- Scripps Clinic, Torrey Pines
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
30 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients 30 years of age or older with the diagnosis idiopathic Parkinson's disease
Description
Inclusion Criteria:
- Is age 30 years or older at the time of onset of Parkinson's
- Has been diagnosed with idiopathic Parkinson's Disease by a Scripps Neurologist
- Is reliable, cooperative and willing to comply with all protocol-specified procedures and/or sub-study if consented or have legal representative/guardian willing to do so
- Able to understand and grant informed consent or have a legal representative/ guardian who is able to do so
Exclusion Criteria:
- Patient has been previously enrolled in The Parkinson's Disease NeuroGenebank at Scripps Clinic Registry
- If a blood draw would be contraindicated for any reason
- Has a significant chronic medical condition (i.e. CVA, hepatic encephalopathy) which, in the investigator's option, may interfere with the patient's optimal participation in the study
- Treatment with any investigational agents or devices within 30 days preceding enrollment in the study
- Has undergone ECT within 90 days preceding enrollment in the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
No Treatment
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There are no interventions in this study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neurogenetic databank
Time Frame: Study completion
|
initiate a Parkinson's disease neurogenetic databank by obtaining blood samples in order to define genes for Parkinson's disease and other neurological conditions.
|
Study completion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cinnamon Bloss, PhD, Scripps Translational Science Institute and Genomic Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2008
Primary Completion (Estimated)
August 1, 2030
Study Completion (Estimated)
August 1, 2030
Study Registration Dates
First Submitted
October 2, 2008
First Submitted That Met QC Criteria
October 2, 2008
First Posted (Estimated)
October 6, 2008
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 15, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HSC# 08-5022
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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