Non Invasive and Non-Contact Imaging Of Tissue Oxygenation and Vascular Reactivity

April 20, 2022 updated by: Chandan K Sen

Non Invasive and Non-Contact Dual-modal Imaging Of Tissue Oxygenation and Vascular Reactivity Dynamic Imaging Of Tissue Metabolism and Vascular Function.

  1. Quantitative validation of non-contact oxygenation imaging by the CWC imaging system
  2. Quantitative validation of non-contact vascular function imaging by the CWC imaging system
  3. Evaluation of the clinical usability of the CWC imaging system for further technology development and engineering improvement

Study Overview

Status

Withdrawn

Detailed Description

The hyperspectral imaging technique estimates cutaneous tissue oxygenation by illuminating tissue and detecting tissue reflectance at different wavelengths. One major advantage of hyperspectral imaging is non-invasive and non-contact detection of tissue functional properties. The dual-mode imaging system integrates hyperspectral and thermal imaging modalities for simultaneous assessment of cutaneous tissue oxygenation and vascular function. This clinical protocol is defined to validate the CWC system on healthy human subjects

Study Type

Observational

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

    • Ohio
      • Columbus, Ohio, United States, 43210
        • The Ohio State University.

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

Sampling Method

Probability Sample

Study Population

Interested healthy volunteers

Description

Inclusion Criteria:

  • Adult 18 years and older
  • No history of diabetes.
  • No history of vascular disease

Exclusion Criteria:

  • Under 18 years of age
  • Unable to provide informed consent
  • Prisoners
  • Current smoker

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
1
Healthy participants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Non-Contact Oxygenation Imagiing
Time Frame: 1 year
Quantitative validation of non-contact oxygenation imaging by the CWC imaging system
1 year
Non-Contact Vascular Function Imaging
Time Frame: 1 year
Quantitative validation of non-contact vascular function imaging by the CWC imaging system
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical usability for Comprehensive Wound Centers
Time Frame: 1 year
Evaluation of the clinical usability of the CWC imaging system for further technology development and engineering improvement.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Chandan K Sen, Ph.D., Ohio State University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 Registration Dates

First Submitted

April 5, 2012

First Submitted That Met QC Criteria

April 5, 2012

First Posted (Estimate)

April 9, 2012

Study Record Updates

Last Update Posted (Actual)

April 28, 2022

Last Update Submitted That Met QC Criteria

April 20, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2010H0017

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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