Abbott: all 1,345 studies

Page 2 of 14. Open to participants first (52), then studies with results posted, then the rest; newest registration first within each.

• XIENCE 28 USA StudyCompletedNCT03815175Not applicableResults posted
• Evaluation of the Infinity Deep Brain Stimulation Electrode Screening Mode ToolCompletedNCT03794661Not applicableResults posted
• CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat Patients With Severe Aortic Stenosis.CompletedNCT03752866Not applicableResults posted
• Advisor HD Grid Observational StudyCompletedNCT03733392Results posted
• An Evaluation of a Multi-target Stool DNA (Mt-sDNA) Test, Cologuard, for CRC Screening in Individuals Aged 45-49 and at Average Risk for Development of Colorectal Cancer: Act NowCompletedNCT03728348Results posted
• FlexNav EU CE Mark StudyCompletedNCT03724812Not applicableResults posted
• Physiologic Pacing RegistryCompletedNCT03719040Results posted
• Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCath SE) Catheter for Ablation of Drug Refractory, Symptomatic, Persistent Atrial FibrillationCompletedNCT03650556Not applicableResults posted
• Intraoperative Investigation of a Directional Lead and Local Field Potentials for the Optimization of Stimulation EfficacyCompletedNCT03630302Results posted
• Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular CalcificationCompletedNCT03539458Not applicableResults posted
• ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI)CompletedNCT03507777Not applicableResults posted
• The MitraClip® EXPAND Study of the Next Generation of MitraClip® DevicesCompletedNCT03502811Results posted
• MitraClip NT System Post-marketing Surveillance Study - JapanCompletedNCT03500692Results posted
• Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to 60 Months Suffering From Acute DiarrheaCompletedNCT03473561Phase 3Results posted
• Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants, Children and Adolescents With Acute DiarrheaCompletedNCT03463512Phase 3Results posted
• Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Transcatheter Mitral Valve System for the Treatment of Symptomatic Mitral RegurgitationActive, not recruitingNCT03433274Not applicableResults posted
• A Prospective Observational Program Using Digital Technology Tools to Enhance Patient Adherence to Omacor TherapyCompletedNCT03415152Results posted
• Absorb GT1 Japan PMSCompletedNCT03409731Not applicableResults posted
• Hemodynamic-GUIDEd Management of Heart FailureCompletedNCT03387813Not applicableResults posted
• Clinical Investigation of the Next-Generation Intraocular LensesCompletedNCT03372434Not applicableResults posted
• XIENCE 28 Global StudyCompletedNCT03355742Not applicableResults posted
• TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial FibrillationCompletedNCT03354663Not applicableResults posted
• BurstDR™ micrOdosing stimuLation in De-novo PatientsCompletedNCT03350256Not applicableResults posted
• Abbott Laboratories Alinity s Blood Screening Assays - Clinical Evaluation ProtocolCompletedNCT03285295Not applicableResults posted
• Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therapy During the TrialCompletedNCT03277378Not applicableResults posted
• EnSite Precision Observational StudyCompletedNCT03260244Results posted
• Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Devices Using the CardioMEMS™CompletedNCT03247829Results posted
• TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With Moderate or Greater TRCompletedNCT03227757Not applicableResults posted
• XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HBR Patients.CompletedNCT03218787Not applicableResults posted
• The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption (H070005) Post Approval StudyCompletedNCT03165526Results posted
• Clinical Investigation of the Next-Generation Intraocular LensCompletedNCT03111550Not applicableResults posted
• Multi-center Prospective Study Determining the Sustainability of Pain Relief and Psychosocial and Functional Responses When Utilizing a Multiple Waveform Enabled NeurostimulatorCompletedNCT03082261Not applicableResults posted
• Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alternative AccessCompletedNCT03056573Not applicableResults posted
• AMPLATZER Duct Occluder II Additional SizesCompletedNCT03055858Not applicableResults posted
• ABLATOR Brazil - Ablation Observational Study (Registry)CompletedNCT03041233Results posted
• HeartMate 3 CE Mark Study Long Term Follow-upCompletedNCT03022461Results posted
• Trifecta™ GT Post Market Clinical Follow-upCompletedNCT03016169Not applicableResults posted
• Clinical Evaluation of the Infinity Deep Brain Stimulation SystemCompletedNCT02989610Results posted
• CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming StrategiesCompletedNCT02986074Not applicableResults posted
• AMPLATZER™ LAA Occluder Post Approval Study (PAS)CompletedNCT02964208Results posted
• IPG Replacement Study (PREFERENCE-H)CompletedNCT02963259Results posted
• CardioMEMS HF System OUS Post Market StudyCompletedNCT02954341Results posted
• AMPLATZER™ Cardiac Plug Observational Post-Approval StudyCompletedNCT02954237Results posted
• Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord StimulationCompletedNCT02950831Not applicableResults posted
• PRESSUREwire StudyCompletedNCT02935088Results posted
• Burst Optimized Stimulation StudyCompletedNCT02896361Not applicableResults posted
• MOMENTUM 3 Continued Access ProtocolCompletedNCT02892955Not applicableResults posted
• AMPLATZER™ Amulet™ LAA Occluder TrialCompletedNCT02879448Not applicableResults posted
• A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD System on Patients Undergoing Magnetic Resonance ImagingCompletedNCT02877693Not applicableResults posted
• Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients Without Antiplatelet TherapyCompletedNCT02836652Phase 4Results posted
• MultiPoint Pacing™ Post Market StudyCompletedNCT02832622Results posted
• SJM MRI Diagnostic Imaging Registry (IDE)CompletedNCT02807948Not applicableResults posted
• Clinical Investigation iDesign System With 1.3-PRESBY Treatment and STAR S4 IR™ Excimer Laser SystemTerminatedNCT02806726Not applicableResults posted
• TARGET Post-Approval StudyCompletedNCT02800863Results posted
• Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With FIRM Guided ProceduresCompletedNCT02799043Not applicableResults posted
• A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE StudyCompletedNCT02787291Not applicableResults posted
• Clinical Investigation of the Bacterially-Derived Healon5 Ophthalmic Viscosurgical Device (OVD)CompletedNCT02782676Not applicableResults posted
• Concordance of Key Actionable Genomic Alterations as Assessed in Tumor Tissue and Plasma in Non Small Cell Lung CancerTerminatedNCT02762877Results posted
• EnSite Precision™ 2.0 RegistryCompletedNCT02757430Results posted
• A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditional SCS SystemsCompletedNCT02738840Not applicableResults posted
• EGM Analysis in Idiopathic Outflow Tract Ventricular ArrhythmiaCompletedNCT02722577Results posted
• FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal Atrial Fibrillation (PAF)TerminatedNCT02703454Not applicableResults posted
• CardioMEMS European Monitoring Study for Heart FailureCompletedNCT02693691Not applicableResults posted
• Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced Wavescan Studio™ System and Star S4 IR™CompletedNCT02675751Not applicableResults posted
• FreeStyle Libre in Pregnancy StudyCompletedNCT02665455Not applicableResults posted
• Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Lens (IOL)CompletedNCT02649842Not applicableResults posted
• A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of the ALK HDM Tablets in Adult Subjects With HDM-Induced Allergic Rhinitis and/or Atopic AsthmaCompletedNCT02596321Phase 3Results posted
• Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back PainCompletedNCT02587637Not applicableResults posted
• Advanced Bradycardia Device Feature Utilization and Clinical Outcomes IICompletedNCT02577887Results posted
• AF Substrate Mapping and Guided AblationCompletedNCT02571218Not applicableResults posted
• Post-Approval Study of the Tecnis® Toric IOLCompletedNCT02566083Not applicableResults posted
• Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee (BTK) Lesions - A Pilot StudyCompletedNCT02561299Not applicableResults posted
• Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE) StudyCompletedNCT02548455Not applicableResults posted
• AVJ-514 Japan TrialCompletedNCT02520310Not applicableResults posted
• XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveillance (XIENCE Xpedition SV Japan PMS)CompletedNCT02513732Results posted
• XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveillance (XIENCE PRIME SV Japan PMS)CompletedNCT02513719Results posted
• HeartMate 3 ELEVATE™ RegistryCompletedNCT02497950Results posted
• A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg Daily Versus Crinone 8% Intravaginal Progesterone Gel 90 mg Daily for Luteal Support in In-Vitro Fertilization (LOTUS II)CompletedNCT02491437Phase 3Results posted
• Quartet Lead and Resynchronization Therapy Options III (QUARTO_III)CompletedNCT02476201Not applicableResults posted
• OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiography to Guide Coronary Stent ImplantationCompletedNCT02471586Not applicableResults posted
• MediGuide RegistryTerminatedNCT02470312Results posted
• SHIELD II Clinical InvestigationTerminatedNCT02468778Not applicableResults posted
• Amplatzer™Amulet™ Post-Market Study (Amulet™PMS)CompletedNCT02447081Results posted
• Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insufficiency Due to Cystic FibrosisCompletedNCT02415959Phase 2Results posted
• Topera C-FIRM RegistryCompletedNCT02407249Results posted
• Abbott Sensor Based Glucose Monitoring System Paediatric StudyCompletedNCT02388815Not applicableResults posted
• Topera E-FIRM RegistryCompletedNCT02386345Results posted
• Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Virus Strains for the Southern Hemisphere 2015 SeasonCompletedNCT02381418Phase 3Results posted
• A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiveness and Safety of Lactulose Retention Enema in the Treatment of Cirrhotic Patients With Grade 3 or 4 (West Haven Criteria) Hepatic Encephalopathy (HE) [The RETRO Study]CompletedNCT02377947Results posted
• Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese Patients With Chronic Heart FailureCompletedNCT02367716Results posted
• HF Assessment With BNP in the Home: Part IITerminatedNCT02351063Not applicableResults posted
• A Post Market Cohort With the Spinal Modulation Neurostimulator System in Peripheral NeuropathyTerminatedNCT02349646Results posted
• A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG stimulatiOn in the Nordic RegionTerminatedNCT02346643Results posted
• ABLATOR Ablation Observational RegistryCompletedNCT02344173Results posted
• Coronary Flow Reserve Following Orbital AtherectomyCompletedNCT02339545Results posted
• A Post Market Study to Assess the Spinal Modulation Neurostimulator System for Chronic Intractable PainCompletedNCT02335502Results posted
• A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurostimulator System for the Management of Chronic Neuropathic Pain of the Foot and/or Lower LegTerminatedNCT02335489Results posted
• A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimulator System in Chronic Post Surgical PainTerminatedNCT02335229Results posted
• A Post Market Study on Dorsal Root Ganglion (DRG) Stimulation in Failed Back Surgery Syndrome (FBSS)TerminatedNCT02335216Results posted
• Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STEMI Patients Undergoing Primary PCICompletedNCT02325973Not applicableResults posted

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