- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06781411
Unity Cures Future (UCF) Biobank
Unity Cures Future (UCF) Biobank for Translational & Biomedical Research At UCF College of Medicine and Burnett School of Biomedical Sciences with Identifiable Human Tissue.
Study Overview
Status
Conditions
Detailed Description
The goal of this human tissue repository protocol is to aggregate resources and streamline the acquisition of human tissue. It is optimal for the advancement of biomedical and translational medical research that the human tissue be received under one protocol by the College of Medicine's the Clinical & Aerospace Health Research team and transferred to the COM/BSBS research scientists for laboratory testing.
This aggregation of efforts and resources through a human tissue repository protocol allows for:
- Improvements in biomedical and translational medical research by availability of viable human tissues.
- Reduced recruitment and enrollment burden on the Clinical & Aerospace Health Research team and the participants via pooled recruitment. Further, participants will only need to provide one informed consent. Received human tissue may be used for multiple protocols.
- Improved data for analysis as participants will complete an online case report form containing basic demographic data; planned location and date of upcoming surgery or procedure; diagnosis; name of surgeon/doctor for the planned surgery or procedure; type of surgery or procedure; medical data; medical history; and surgery history.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Britney-Ann Wray, BS, CTBS, CCRP
- Phone Number: 4072668742
- Email: britney-ann.wray@ucf.edu
Study Locations
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Florida
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Orlando, Florida, United States, 32827
- Recruiting
- University of Central Florida
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Contact:
- Amoy Fraser, PhD, CCRP, PMP
- Phone Number: 4072668742
- Email: Amoy.Fraser@UCF.edu
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Contact:
- Amoy Fraser, PhD, CCRP, PMP
-
Contact:
- Britney-Ann Wray, BS, CTBS, CCRP
- Phone Number: 4072668742
- Email: britney-ann.wray@ucf.edu
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- be able to read and understand English
- scheduled for a surgery or procedure that will result in the removal of human tissue.
Exclusion Criteria:
- Pregnant
- unable to provide an informed consent
- unable to understand or read in English
- minors (ages under 18)
- prisoners
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Donated Human Tissue
This Project will receive discarded human tissue from consented participants.
For the purposes of this project, human tissue is defined as any bodily material collected from a human person, including bone marrow, skin, tumors, etc., through a clinical procedure.
The clinical procedure will done not be done solely for the purpose of this Project.
Participants (donors) will prospectively provide informed consent, complete an online case report form, and donate the unwanted human tissue that results from their surgery/procedure.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Receipt of donated human tissue for research
Time Frame: 50 years
|
The key research divisions are cancer, cardiovascular, immunity and pathogenesis, neuroscience, and molecular microbiology.
Frequently, these studies require human tissue for testing of assays and devices.
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50 years
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
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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