- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06084312
Contact Registry for Clinical Trials
Contact Registry for Clinical Trials At the University of Central Florida College of Medicine
The purpose of the Contact Registry for Clinical Trials is to develop a database/listserv of persons interested in clinical trials occurring at the University of Central Florida College of Medicine.
Sign up for the UCF College of Medicine's Contact Registry for Clinical Trials to learn about clinical research and clinical trials in areas of interest to you!
https://ucf.qualtrics.com/jfe/form/SV_do4WGvKlz4f8Wwe
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
Florida
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Orlando, Florida, United States, 32816
- Recruiting
- University of Central Florida
-
Contact:
- Amoy Fraser, PhD, CCRP, PMP
- Phone Number: 4072668742
- Email: Amoy.Fraser@UCF.edu
-
Contact:
- Erica Martin, BS
- Phone Number: 4072668742
- Email: erica.martin@ucf.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 18 years of age or older
- Persons who do not read English could register through the assistance of their friends or software for translation
Exclusion Criteria:
- Children may not register
- Persons who are unable to consent may not register
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
This registry will not target any specific populations
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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To allow persons to sign up to learn more about clinical trials and clinical research around certain medical indications that will be occurring at the University of Central Florida College of Medicine
Time Frame: 1 year
|
1 year
|
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- STUDY00004132
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.