Analysis of the Vascular Pattern of the Superficial Temporal Artery
March 21, 2014 updated by: University Hospital Tuebingen
In Vivo Analysis of the Vascular Pattern of the Superficial Temporal Artery Based on Digital Subtraction Angiography
Retrospective analysis to the course and branching pattern as well as surgically relevant inner diameters and lengths of the superficial temporal artery (STA) by digital subtraction angiographies (DSA).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
93
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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Tuebingen, Germany, 72076
- Clinic for Hand, Plastic and Reconstructive Surgery with Burn Center BG Trauma Center
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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
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
clinic patients who underwent digital subtractions angiographie
Description
Inclusion Criteria:
- good quality digital subtractions angiographies of the STA
Exclusion Criteria:
- bad quality digital subtractions angiographies of the STA
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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Vascular pattern 1
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Vascular pattern 2
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Vascular pattern 3
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Vascular pattern 4
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Vascular pattern 5
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Vascular pattern 6
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Vascular pattern 7
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Vascular pattern 8
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Vascular pattern 9
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Vascular pattern 10
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Vascular pattern 11
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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vessel diameters
Time Frame: up to 36 month
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up to 36 month
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
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vessel length
Time Frame: up to 36 months
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up to 36 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
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
January 1, 2011
Primary Completion (Actual)
February 1, 2013
Study Completion (Actual)
February 1, 2013
Study Registration Dates
First Submitted
March 19, 2014
First Submitted That Met QC Criteria
March 21, 2014
First Posted (Estimate)
March 26, 2014
Study Record Updates
Last Update Posted (Estimate)
March 26, 2014
Last Update Submitted That Met QC Criteria
March 21, 2014
Last Verified
March 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- BGU-001
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.