- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01182584
Application of Digital Infrared Thermal Imaging (DITI) in Graves' Disease
December 21, 2010 updated by: National Taiwan University Hospital
Application of Digital Infrared Thermal Imaging in Thyroid Disease and Associated Ophthalmopathy and Dermopathy
Graves' disease is characterized by thyrotoxicosis, goiter, ophthalmopathy and dermopathy.
Pathogenesis involves autoimmune process.
The investigators think temperatures of the area involved in the inflammation may change.
Thus the investigators plan to take temperature pictures of Graves' patients using digital infrared thermal imaging system and observe the change.
Study Overview
Status
Unknown
Conditions
Detailed Description
We will recruited patients of Graves' disease from out patient clinics.
We will perform thyroid echo and soft tissue echo first.
Then we let patients sit before the thermal camera and take thermal images of eyes necks and tibia.
After data collection, we analyse the relation between temperature and laboratory data such as thyroid function and autoimmune profiles.
Study Type
Observational
Enrollment (Anticipated)
200
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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Taipei, Taiwan
- Recruiting
- National Taiwan University
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Contact:
- Shyang-Rong Shih, M.D.
- Phone Number: 0972653337
- Email: srshih@ntu.edu.tw
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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
16 years to 60 years (ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Graves' disease patients with or without ophthalmopathy and dermopathy
Description
Inclusion Criteria:
- Graves' disease patients. Healthy people
Exclusion Criteria:
- Pregnancy. <16 years old or > 60 years old
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 |
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Healthy volunteers
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Graves' disease
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Shyang-Rong Shih, National Taiwan University
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
December 1, 2009
Primary Completion (ANTICIPATED)
October 1, 2011
Study Completion (ANTICIPATED)
December 1, 2011
Study Registration Dates
First Submitted
August 12, 2010
First Submitted That Met QC Criteria
August 16, 2010
First Posted (ESTIMATE)
August 17, 2010
Study Record Updates
Last Update Posted (ESTIMATE)
December 22, 2010
Last Update Submitted That Met QC Criteria
December 21, 2010
Last Verified
December 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 200811040R
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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