In-vivo Optical Coherence Tomography Imaging in Dermatooncology
NCT ID: NCT01680562
Last Updated: 2012-09-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
37 participants
OBSERVATIONAL
2010-01-31
2012-12-31
Brief Summary
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A total of 70 malignant skin lesions was evaluated during this prospective pilot study. Diagnoses based on OCT imaging as an additional diagnostic tool, were compared to those based on the clinical standard pathway at the Department of Dermatology, Medical University of Vienna. For the purpose of this study, the histopathological diagnosis was used as the reference diagnostic standard.
The major aims of this study is the investigation of the ability of ultrahigh resolution OCT to identify fine morphological characteristics associated with basal cell carcinoma, actinic keratosis, superficial squamous cell carcinoma, seborrheic keratosis, melanocytic nevi and melanoma.
* To correlate the morphologic features identified with ultrahigh resolution OCT with routine histopathology
* To investigate the clinical feasibility of ultrahigh resolution and spectroscopic OCT technology
* To assess the effectiveness of ultrahigh resolution and spectroscopic OCT imaging to diagnose various melanocytic and non-melanocytic skin tumors
* To compare the diagnostic capabilities of ultrahigh resolution OCT with standard non-invasive diagnostic procedures such as epiluminescence microscopy
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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skin cancer
Skin cancer patients with scheduled tumor excision and subsequent histopathological analysis of the tumor.
in-vivo skin tumor imaging via optical coherence tomography
optical coherence tomography imaging of skin lesion; digital dermoscopy imaging of skin lesion
Interventions
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in-vivo skin tumor imaging via optical coherence tomography
optical coherence tomography imaging of skin lesion; digital dermoscopy imaging of skin lesion
Eligibility Criteria
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Inclusion Criteria
* nevi
* dermatofibroma
* basal cell carcinoma
* actinic keratosis
* squamous cell carcinoma
* Bowen's disease
* Merkel cell carcinoma
* malignant melanoma
Exclusion Criteria
* patients during compulsory military service
* patients with an appointed guardian
18 Years
ALL
Yes
Sponsors
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Medical University of Vienna
OTHER
Responsible Party
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Jessika Weingast, MD
Principal Investigator
Principal Investigators
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Michael Binder, MD
Role: PRINCIPAL_INVESTIGATOR
Medical University of Vienna
Locations
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Department of Dermatology, Medical University of Vienna
Vienna, , Austria
Countries
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Other Identifiers
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201880
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
1126/2009
Identifier Type: -
Identifier Source: org_study_id