- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01333553
Monitoring the Response of Port Wine Stain Birthmarks to Laser Therapy With Wide-field Functional Imaging Technologies
October 28, 2022 updated by: Beckman Laser Institute and Medical Center, University of California, Irvine
Monitoring the Response of Port Wine Stain Birthmarks to Laser Therapy With Wide-field
The researcher develop non-invasive imaging modalities for assessment of port wine stain during laser therapy treatment of Port Wine Stain.
The imaging modalities will be used to guide immediate retreatment of regions of persistent perfusion during the procedure.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The researcher can use imaging system operates by projecting low-power near-infrared structured light patterns on to the tissue of interest in a non-contact, reflection geometry and then capturing the reflectance with a camera.The system can image the depth-resolved optical properties of in-vivo tissues, allowing rapid, non-invasive visualization of sub-surface structures of Port Wine Stain.
Study Type
Observational
Enrollment (Actual)
69
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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California
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Irvine, California, United States, 92612
- Beckman Laser Institute Medical Clinic
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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
1 day and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Study population will be selected from an outpatient population with Port Wine Stain birthmark at Beckman Laser Institute and Medical Clinic, University of California, Irvine.
Patients with Port Wine Stain birthmark will be candidates for participation.
Description
Inclusion Criteria:
- All minors, birth to 18 years of age or older with Port Wine Stain birthmark
- Ability to understand and carry out subject instructions
- Sign photograph release form
Exclusion Criteria:
- Inability to understand and/or carry out instructions
- Pregnant women
- Do not sign photograph release form
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Image-guided remove Port Wine Stain
Image-guided surgery remove Port Wine Stain
|
Image-guided surgery remove Port Wine Stain
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Image-guided surgery remove Port Wine Stain
Time Frame: 24 hours
|
Image-guided surgery remove Port Wine Stain
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Bernard Choi, PhD, Beckman Laser Institute University of California Irvine
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
April 1, 2010
Primary Completion (Actual)
April 1, 2018
Study Completion (Actual)
April 1, 2018
Study Registration Dates
First Submitted
August 3, 2010
First Submitted That Met QC Criteria
April 8, 2011
First Posted (Estimate)
April 12, 2011
Study Record Updates
Last Update Posted (Actual)
November 1, 2022
Last Update Submitted That Met QC Criteria
October 28, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20107376
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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