- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01557205
Research and System Development on Functional 3D Optical Tomography for Skin Cell Imaging
March 16, 2012 updated by: National Taiwan University Hospital
The investigators will obtain human skin specimen (sized approximately 1 cm x 1 cm) for dermatological surgical patients in National Taiwan University Hospital, after informed consent was obtained.
Human skin keratinocytes, fibroblasts, and melanocytes will be cultured from the human skin specimen.
The three dimensional images of these cultured cells will be observed by a ultra-high resolution 3-dimensional optical coherence tomography.
Study Overview
Status
Unknown
Conditions
Detailed Description
The investigators will obtain human skin specimen (sized approximately 1 cm x 1 cm) for dermatological surgical patients in National Taiwan University Hospital, after informed consent was obtained.
Human skin keratinocytes, fibroblasts, and melanocytes will be cultured from the human skin specimen.
The three dimensional images of these cultured cells will be observed by a ultra-high resolution 3-dimensional optical coherence tomography.
Study Type
Observational
Enrollment (Anticipated)
30
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Aged between 20 to 100.
People who received benign skin tumor removal in dermatological surgical unit.
OR people who received skin grafts (full thickness or split thickness) for reconstruction of surgical wounds after removing malignant skin cancer.
Description
Inclusion Criteria:
- Aged between 20 to 100.
- People who received benign skin tumor removal in dermatological surgical unit. OR
- People who received skin grafts (full thickness or split thickness) for reconstruction of surgical wounds after removing malignant skin cancer.
Exclusion Criteria:
- Age less than 20 years old,
- Psychiatric patients,
- Pregnant women.
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?
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
March 1, 2012
Primary Completion (Anticipated)
April 1, 2013
Study Completion (Anticipated)
April 1, 2013
Study Registration Dates
First Submitted
March 15, 2012
First Submitted That Met QC Criteria
March 16, 2012
First Posted (Estimate)
March 19, 2012
Study Record Updates
Last Update Posted (Estimate)
March 19, 2012
Last Update Submitted That Met QC Criteria
March 16, 2012
Last Verified
March 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 201202019RIC
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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