Arteria Temporalis SuperficialisNCT02096497
Analysis of the Vascular Pattern of the Superficial Temporal Artery
An observational study of Arteria Temporalis Superficialis, run by University Hospital Tuebingen at 1 site in Germany.
Trial summary
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). Read more about this study
- Who is it for?
- Ages 18 to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Arteria Temporalis Superficialis
- How many people
- 93 participants
- Where
- 1 siteGermany
- Study dates
- Jan 2011to Feb 2013
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: clinic patients who underwent digital subtractions angiographie
Who may be able to join
- good quality digital subtractions angiographies of the STA
Who cannot join
- bad quality digital subtractions angiographies of the STA
Trial locations and contacts
1 site in 1 country.
Germany1 site
Clinic for Hand, Plastic and Reconstructive Surgery with Burn Center BG Trauma Center
Tübingen, 72076
About this study
Official title: 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).
- Conditions
- Arteria Temporalis Superficialis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Vascular pattern 1 | Not described | |
| Vascular pattern 2 | Not described | |
| Vascular pattern 3 | Not described | |
| Vascular pattern 4 | Not described | |
| Vascular pattern 5 | Not described | |
| Vascular pattern 6 | Not described | |
| Vascular pattern 7 | Not described | |
| Vascular pattern 8 | Not described | |
| Vascular pattern 9 | Not described | |
| Vascular pattern 10 | Not described | |
| Vascular pattern 11 | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
vessel diameters
Measured: up to 36 month
Secondary outcomes (1)
vessel length
Measured: up to 36 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Mar 2014 (estimated)
- Study startJan 2011
- Primary completionFeb 2013
- Study completionFeb 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Arteria Temporalis SuperficialisStudies of the same condition, open and under way.
- More trials run by University Hospital TuebingenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 93 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital Tuebingen
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02096497
- Sponsor's protocol ID
- BGU-001
- Status last verified
- Mar 2014
- First submitted
- 19 Mar 2014
- Last updated
- 26 Mar 2014
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Pinar YA, Govsa F. Anatomy of the superficial temporal artery and its branches: its importance for surgery. Surg Radiol Anat. 2006 Jun;28(3):248-53. doi: 10.1007/s00276-006-0094-z. Epub 2006 Mar 28.
PubMed 16568216
Study at a glance
From the registry record, last updated by the sponsor on 26 Mar 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- In Vivo Analysis of the Vascular Pattern of the Superficial Temporal Artery Based on Digital Subtraction Angiography
- ClinicalTrials.gov ID
- NCT02096497
- Acronym / sponsor ID
- BGU-001
- Conditions
- Arteria Temporalis Superficialis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 93 participants (actual)
- Lead sponsor
- University Hospital TuebingenUniversity, hospital or other
- Study start
- Jan 2011
- Primary completion
- Feb 2013 (actual)
- Study completion
- Feb 2013 (actual)
- First posted
- 26 Mar 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 11
| Arm | Type | Receives |
|---|---|---|
| Vascular pattern 1 | – | – |
| Vascular pattern 2 | – | – |
| Vascular pattern 3 | – | – |
| Vascular pattern 4 | – | – |
| Vascular pattern 5 | – | – |
| Vascular pattern 6 | – | – |
| Vascular pattern 7 | – | – |
| Vascular pattern 8 | – | – |
| Vascular pattern 9 | – | – |
| Vascular pattern 10 | – | – |
| Vascular pattern 11 | – | – |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- clinic patients who underwent digital subtractions angiographie
Key inclusion criteria (1 listed)
- good quality digital subtractions angiographies of the STA
Key exclusion criteria (1 listed)
- bad quality digital subtractions angiographies of the STA
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
vessel diameters
Time frame: up to 36 month
1 secondary outcome
vessel length
Time frame: up to 36 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Mar 2014.
- Background: PubMed 16568216Pinar YA, Govsa F. Anatomy of the superficial temporal artery and its branches: its importance for surgery. Surg Radiol Anat. 2006 Jun;28(3):248-53. doi: 10.1007/s00276-006-0094-z. Epub 2006 Mar 28.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Arteria Temporalis Superficialis, run by University Hospital Tuebingen at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Mar 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
vessel diameters (time frame: up to 36 month). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02096497, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2014.