- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00727480
Finger Imaging to Detect Blood Flow in the Fingertips
June 1, 2015 updated by: Paul L. Carson Ph.D, University of Michigan
Finger Imaging and Biometric System
The purpose of this study is to develop a small, easily used device to detect a person's blood flow in their fingertips.
Study Overview
Detailed Description
To develop a hand held touch-pad device for identification of individuals, to help with banking and, possibly for detection of anxiety.
This is done by their fingerprint and, other digital anatomy and vascular biometrics.
Study Type
Interventional
Enrollment (Actual)
13
Phase
- Not Applicable
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
-
-
Michigan
-
Ann Arbor, Michigan, United States, 48109
- University of Michigan Health System
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Adult male and female who can give informed consent
Exclusion Criteria:
- Under the age of 18
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
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: A
Ultrasound Imaging of fingertips
|
Ultrasound scanning of fingertips for assessment of possible imaging modes with Gray scale ultrasound, color flow vascularity imaging, and color flow vascularity imaging before and after exercise.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To develop a new type of electronic hand held device, that will demonstrate the image quality comparable to existing devices based on optical techniques.
Time Frame: 2002-2011
|
2002-2011
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Paul L. Carson, Ph.D., University of Michigan
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
September 1, 2002
Primary Completion (Actual)
July 1, 2008
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
July 30, 2008
First Submitted That Met QC Criteria
July 31, 2008
First Posted (Estimate)
August 4, 2008
Study Record Updates
Last Update Posted (Estimate)
June 3, 2015
Last Update Submitted That Met QC Criteria
June 1, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2002-0535
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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