Arkansas Heart Hospital

Little Rock, Arkansas 72211

6 studies enrolling now · 88 studies all time

What they study most

Acute Coronary Syndrome, Acute Myocardial Infarction, Adverse Effect of MRI on an Implanted Pacemaker, Adverse Effect of MRI on an Implanted Pacemaker Lead, Anemia, Aortic Valve Disease, Aortic Valve Stenosis, Arrhythmias, Cardiac, Arterial Embolism, Arterial Occlusive Disease, Atherosclerosis, Atrial Arrhythmia

Studies at this site

• THRIVE- THerapeutic IntravasculaR Ultrasound (TIVUS™) REnal Denervation System Versus Sham for the Adjunctive Treatment of Hypertension — Recruiting now
• Study of the Shockwave Medical SkyRunner Carotid Intravascular Lithotripsy (IVL) System for the Treatment of Calcified Carotid Arteries Prior to Trans-Carotid Stenting (SKYWARD Trans-Carotid IDE [Investigational Device Exemption] Study) — Recruiting now
• SELUTION4BTK Trial — Recruiting now
• Abbott Vascular Medical Device Registry — Recruiting now
• Impella RP Flex with Smart Assist — Recruiting now
• VOLT-AF IDE Clinical Study — Completed
• TECTONIC CAD IVL IDE Study — Running, not enrolling
• A Study of Milvexian in Participants After a Recent Acute Coronary Syndrome — Completed
• A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillation — Running, not enrolling
• A Prospective Single-Arm Multicenter StuDy of the BarE TEmporary SPur StEnt System foR the tREatment of Vascular Lesions Located in the infrapoplitEal Arteries beLow the Knee (DEEPER REVEAL) — Completed
• A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF: — Completed
• Aveir DR i2i Study — Completed
• REDUCED 1 - Renal Denervation Using Ultrasonic Catheter EmitteD Energy Study / — Running, not enrolling
• ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic Valve Implantation — Enrolling by invitation
• JETi Lower Extremity Venous Thrombosis — Completed
• Left Atrial Appendage Exclusion for Prophylactic Stroke Reduction Trial — Running, not enrolling
• Impella ECP Study (ECP Study) and Impella ECP Continued Access Protocol — Enrolling by invitation
• XIENCE Skypoint Large Vessel Post Approval Study — Running, not enrolling
• Amplitude Vascular Systems (AVS) Lithotripsy POWER PAD 2 Trial — Running, not enrolling
• SELUTION4SFA Trial — Running, not enrolling
• LIFE-BTK Randomized Controlled Trial — Running, not enrolling
• Amulet™ ADVANCE LAA — Running, not enrolling
• Hemodynamic-GUIDEd Management of Heart Failure — Completed
• MitraClip EXPAND G4 Study — Running, not enrolling
• National Cardiogenic Shock Initiative — Completed
• CanGaroo® Registry Study — Completed
• AVEIR Remote Care System Non-Significant Risk Study — Completed
• The DETOUR 2 Clinical Trial — Completed
• AMPLATZER™ Amulet™ LAA Occluder Trial — Completed
• FUnctional diagnoSIs of corONary Stenosis (FUSION) — Completed
• Patient Preferences for Leadless Pacemakers — Completed
• Impella Real-World Surveillance of Patients Using Sodium Bicarbonate — Completed
• Temsirolimus Alone or Paired With Dexamethasone Delivered to the Adventitia to eNhance Clinical Efficacy After Femoropopliteal Revascularization — Stopped early
• Randomized Placebo-controlled Trial of FCM as Treatment for Heart Failure With Iron Deficiency / and Sub-Study — Completed
• The DES BTK Vascular Stent System vs PTA in Subjects With Critical Limb Ischemia — Completed
• Shockwave Medical Peripheral Lithoplasty System Study for PAD (Disrupt PAD III) — Completed
• XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort — Completed
• TactiFlex Paroxysmal Atrial Fibrillation IDE Trial — Completed
• Absorb IV Randomized Controlled Trial — Completed
• TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation — Completed
• ABSORB III Randomized Controlled Trial (RCT) — Completed
• Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbital Atherectomy vs. Conventional Angioplasty Technique Prior to Implantation of Drug-Eluting StEnts: The ECLIPSE Trial — Running, not enrolling
• Obtain Additional Information on Use of CorMatrix ECM (Extracellular Matrix) — Completed
• Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes — Completed
• Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Intervention: REACH PVI — Completed
• Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely Calcified Coronary Lesions (MACE) — Completed
• Pantheris Atherectomy Treatment of In-Stent Restenosis In Lower Extremity Arteries — Completed
• OPTIMIZE IDE for the Treatment of ACS — Stopped early
• REPRISE IV: LOTUS Edge Valve System in Intermediate Surgical Risk Subjects — Stopped early
• XIENCE 28 USA Study — Completed