What this study is
A retrospective and prospective registry of patients admitted for stroke and evidence of Vertebral Artery Origin Stenosis (VAOS).
What's being tested
- Observational Prospective Registry
Intervention · OTHER
This is a prospective registry looking at patients admitted for stroke with evidence of Vertebral Artery Origin Stenosis. Patients clinical outcomes will be collected at 30 days and 1-year post-treatment and angiographic outcomes at 1-year post-treatment
Study details
- Sponsor
- St. Louis University
- Conditions
- Vertebral Artery Stenosis
- Enrolling
- 150 people
- Starts
- 2019-11-19
- Est. completion
- 2026-12
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 90 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Patients between 18 and 90 years of age
- Patient has experienced a posterior circulation ischemic event
- Patient has angiographically confirmed bilateral vertebral artery origin disease (Hypoplasia, occlusion, or stenosis).
- Patient has >50% stenosis on the side being targeted for therapy
You can't join if
- Pregnant women
- Contrast Indication to the use of anti-platelet drugs
- There is tandem vertebral or basilar artery stenosis
- The serum creatinin is >2.5
- Baseline modified Rankin score is >3
- < 5 years life expectancy
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (10)
10 openBaptist Medical Center Jacksonville
Jacksonville, Florida, United States
- Nancy Ebreo, CCRC,RRT,CRA · ContactNancy.ebreo@bmcjax.com
- Nima Aghaebrahim, MD · Principal investigator
RecruitingUniversity of Southern Florida
Tampa, Florida, United States
- Waldo Guerrero, MD · Contactwrguerre@usf.edu
- Amy Denardo · Contactamydenardo@usf.edu
- Waldo Guerrero, MD · Principal investigator
RecruitingNorthwestern Medicine Regional Medical Group
Winfield, Illinois, United States
- Dhruvil Pandya, MD · Contactdhruvil.pandya2@nm.org
- Dhruvil Pandya, MD · Principal investigator
RecruitingUniversity of Iowa
Iowa City, Iowa, United States
- Santiago Ortega, MD, MS · Contactsanty-ortega@uiowa.edu
- Santy Ortega-Gutierrez, MD · Principal investigator
RecruitingSSM DePaul Hospital
Bridgeton, Missouri, United States
- Makenzie Woodford, BS · Contact+1 (314) 344-6195makenzie.woodford@ssmhealth.com
- Amer Alsheklee, MD · Principal investigator
RecruitingSaint Louis University
St Louis, Missouri, United States
- Kara Christopher, MS, MPH, PhD · Contact314-977-3211andre.guthrie@health.slu.edu
- Benjamin Cummins, MPH/MPA · Contact314-977-3229benjamin.cummins.1@health.slu.edu
- Randall Edgell, MD · Principal investigator
RecruitingCleveland Clinic
Cleveland, Ohio, United States
- Lauren Todd · Contact216-442-5676TOODL2@ccf.org
- Gabor Toth, MD · Principal investigator
Not yet recruitingMercy Health Neuroscience Institute
Toledo, Ohio, United States
- Kristine Below · ContactKBelow@mercy.com
- Osama Zaidat, MD · Principal investigator
RecruitingSemmes Murphey Clinic
Memphis, Tennessee, United States
- Amanda Nolte · Contactannolte@semmes-murphey.com
- Lucas Elijovich, MD · Principal investigator
RecruitingTexas Tech University Health Science Center of El Paso
El Paso, Texas, United States
- Israel Alba · Contactisrael.alba@ttuhsc.edu
- Vikas Gupta, MD · Principal investigator
Not yet recruiting
Study team
Sponsor
St. Louis University
Study ID 29760
Principal investigator
Randall Edgell, MD
St. Louis University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.