Prospective Outcomes Study: Vectra® DA Guided Care Compared to Usual Care
NCT02832297
Recruiting
In this 12-month multi-center prospective, site-randomized, two-arm trial, approximately 318 biologic-naïve subjects with RA who are candidates for treatment intensification due to inadequate response to MTX monotherapy will be enrolled at up to 60 study sites.
Gender:
All
Ages:
Between 18 years and 80 years
Trial Updated:
07/27/2018
Locations: Paramount Medical Research, LLC, Middleburg Heights, Ohio
Conditions: Arthritis, Rheumatoid
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TARGET Intracranial Aneurysm Coiling Registry
NCT01748903
Recruiting
The purpose of this prospective registry is to collect real world, post-marketing data on the use of Stryker Target® 360,Target® 2D, and 2nd generation Target® Nano coils for the embolization of ruptured or unruptured intracranial saccular aneurysms. Up to 300 patients (150 in the TARGET 360°/Helical arm and 150 in the New NANO arm) presenting with intracranial aneurysms suitable for coil embolization will be enrolled at up to 20 sites. A post hoc analysis comparing Target® 360° and Target® 2D c... Read More
Gender:
All
Ages:
18 years and above
Trial Updated:
07/20/2018
Locations: Mercy Health St. Vincent Medical Center, Toledo, Ohio
Conditions: Intracranial Aneurysms
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Microbiome and Bariatric Surgery
NCT03065426
Recruiting
This is a prospective, 24-month, longitudinal study of patients planning to undergo bariatric surgery (Roux-en-Y Gastric Bypass or Sleeve Gastrectomy) in which we aim to identify correlates and predictors of observed weight loss trajectories following bariatric surgery. This approach will expand current knowledge by examining the combined impact of empirically supported behavioral and biological data in a large sample over time. Intensive measurement of problematic eating behaviors, mood, and co... Read More
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
05/12/2017
Locations: Cleveland Clinic, Cleveland, Ohio
Conditions: Weight Change, Body
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Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction
NCT00673842
Recruiting
This study will assess whether an implantable defibrillator will increase the likelihood of survival in patients who have had a heart attack in the prior 5 years, have abnormal test results from a 24 hour heart monitor, and who have low normal heart function.
Gender:
All
Ages:
Between 18 years and 80 years
Trial Updated:
07/07/2016
Locations: Northeast Ohio Cardiovascular Specialists, Akron, Ohio
Conditions: Myocardial Infarction, Sudden Death
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Transcatheter Aortic Valve Replacement System Pivotal Trial
NCT02163850
Recruiting
Prospective, randomized, unblinded, multi-center investigational study with enrollment at up to 45 investigational sites. The study is designed to compare the study device (Direct Flow Medical Transcatheter Aortic Valve System) composite event rate to a blended commercial comparator (using approved Medtronic self-expanding bioprosthesis or Edwards balloon-expandable bioprosthesis) in high and extreme risk Subjects with severe symptomatic aortic stenosis. Subjects will be followed through the ind... Read More
Gender:
All
Ages:
All
Trial Updated:
04/29/2016
Locations: Ohio Health Riverside Methodist, Columbus, Ohio
Conditions: Aortic Valve Stenosis
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