Baxter Healthcare Corporation: all 171 studies
Page 2 of 2. Open to participants first (4), then studies with results posted, then the rest; newest registration first within each.
- Clinical Performance Comparison of 2 THERANOVA 400 Dialyzer Prototypes in HD With High-Flux Dialyzers in HD and hv HDF ModeCompletedNCT02377622Not applicable
- Comparison of the Clinical Performance of 3 THERANOVA 400 Dialyzer Prototypes With a High-Flux Dialyzer in Hemodialysis ModeCompletedNCT02377570Not applicable
- Necklace-Shaped Sensor for Non-Invasive Remote Monitoring of VitalsCompletedNCT02337790
- Monitoring Subjects With Fluid-Management Issues In the Home EnvironmentCompletedNCT02190877
- Neck-Worn Monitoring Sensor for - A Study for Monitoring Subjects With Fluid-Management Issues During DialysisCompletedNCT02140905
- BDx 7 Day ECG Patch: Electrode Adhesion Clinical StudyCompletedNCT02133261
- Sternal ECG Patch Comparison TrialStatus unknownNCT02126631
- PERCI- Medium Cut Off (MCO)CompletedNCT02084381Not applicable
- Effects of IV Chloride Content on OutcomesCompletedNCT02083198
- Comparison of Continuous Sternal ECG Patch Monitors (Carnation and Zio) TrialStatus unknownNCT02031484
- Evaluation of Evodial Hemodialyzer Selectivity Modifications (Evodial +)CompletedNCT01783626Not applicable
- Performance Comparison of Revaclear With Larger DialyzerCompletedNCT01722695Not applicable
- Oxidized Cellulose hEmostAsis evaluatioNCompletedNCT01637025Not applicable
- Permeability Enhancement to Reduce Chronic InflammationCompletedNCT01582893Not applicable
- HemoControl System Activated in Hemodiafiltration TreatmentsCompletedNCT01582867Not applicable
- High Cut Off Dialysis in Systemic Inflammatory Response Syndrome Patients After Cardiac SurgeryWithdrawnNCT01579396Not applicable
- Comparative Phase 3 Trial to Assess the Safety and Efficacy of Triple-chamber Parenteral Nutrition FormulationCompletedNCT01579097Phase 3
- Improvement of EPO-resistance in Hemodialysis Patients With Chronic Inflammation by High Cut-off HemodialysisCompletedNCT01526798Not applicable
- Cardiac Output Monitoring Managing Intravenous Therapy (COMMIT) to Treat Emergency Department Severe SepsisCompletedNCT01484106Not applicable
- Myoglobin Removal by High Cut-off CVVHDCompletedNCT01467180Not applicable
- e-STEPS: Endotoxin-Associated Sterile Peritonitis Observational StudyCompletedNCT01460056
- Retrospective Analysis of Veritas in Breast ReconstructionCompletedNCT01454713
- Performance of Inductigraft in Spinal FusionCompletedNCT01452022Not applicable
- Veritas in Non-Bridging Ventral Hernia RepairTerminatedNCT01426477
- Survival on Peritoneal Dialysis (PD) Versus Hemodialysis (HD) in ChinaTerminatedNCT01413074Not applicable
- Effect of HCO1100 on Cardiovascular FunctionTerminatedNCT01363921Not applicable
- HepZero:Heparin Free Dialysis With EvodialCompletedNCT01318486Not applicable
- Bronchiectasis: Evaluation of an Educational InterventionWithdrawnNCT01315626
- Safety During Use of Paediatric Triple Chamber Bag FormulasCompletedNCT01304394Phase 3
- Early Progressive Mobility in the CVICU: Assessing Current StatusCompletedNCT01295541
- Air Fluidized Therapy (AFT) in Patients With Suspected Deep Tissue Injury (sDTI)CompletedNCT01292980
- Gambro AK200 ULTRA Hemodiafiltration StudyCompletedNCT01202708Not applicable
- A Pilot Study of a Heparin Dosing Algorithm for HemodialysisCompletedNCT01181544Not applicable
- Efficacy and Time and Resources for Hylenex-facilitated SC Rehydration Versus ORT for Dehydrated Children in the Emergency Department (ED)WithdrawnNCT01120431Phase 4
- Open-label, Randomized Trial to Determine the Effect of Icodextrin Versus Dextrose (Dianeal 2.5%) in HOMA IRWithdrawnNCT01093547Phase 4
- Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar FusionCompletedNCT01018771Not applicable
- Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody FusionCompletedNCT01013389Not applicable
- Bone Graft Materials Observational RegistryTerminatedNCT00974623
- Acute Achilles Repair With or Without OrthADAPT AugmentationWithdrawnNCT00962143Not applicable
- Rotator Cuff Repair (RCR) With and Without OrthoADAPT AugmentationWithdrawnNCT00957255Not applicable
- The Mechanism of Action of Unite Biomatrix in Venous Leg UlcersWithdrawnNCT00953563Not applicable
- Evaluation of Hemodynamic Effects of Cascade Hemofiltration in Septic ShockCompletedNCT00922870Not applicable
- High Cut-Off Continuous Veno-venous Hemodialysis (CVVHD) in Patients Treated for Acute Renal Failure After Systemic Inflammatory Response Syndrome (SIRS)/Septic ShockTerminatedNCT00875888Not applicable
- Evaluation of the Biocompatibility of Cartridge Blood Set Versus Standard Blood LineCompletedNCT00804453Not applicable
- Investigating Modes of Progressive MobilityCompletedNCT00787098Phase 2
- Reduction of Heparin Dose in Dialysis With Evodial SystemCompletedNCT00781690Not applicable
- Pre-Hospital Wireless Transmission of Electrocardiograms to a Cardiologist Via a Hand-Held DeviceCompletedNCT00682526
- Clinical Assessment of a New Catheter Surface Coating With Antimicrobial PropertiesCompletedNCT00621712Not applicable
- Ex Vivo Microbiological Assessment of an Anti-biofilm Catheter in Acute Dialysis ApplicationCompletedNCT00621114Not applicable
- Recompensation of Exacerbated Liver Insufficiency With Hyperbilirubinemia and/or Encephalopathy and/or Renal FailureCompletedNCT00614146Not applicable
- Ease of Use Study for the Gambro Polyflux HD-C4 Small DialyzerCompletedNCT00579202
- Efficacy and Safety Study of Anti-Adhesion Product in the Prevention of Intraperitoneal AdhesionsCompletedNCT00512356Phase 2
- Comparison of the Impact of Dialysis Treatment Type on Patient SurvivalCompletedNCT00510549Phase 4
- Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-Containing Solutions in Post-Surgical Hip Replacement PainCompletedNCT00508495Phase 3
- Analgesic Efficacy, Safety and Tolerability of Two Paracetamol-containing Solutions in Post-Surgical Dental PainCompletedNCT00406679Phase 3
- A Pilot Study of the Envision® SurfaceCompletedNCT00405834
- Envision® Surface EvaluationCompletedNCT00405795
- Effect of Extraneal (Icodextrin)on Triglyceride Levels in PD PatientsWithdrawnNCT00397358Phase 4
- A Crossover Study Assessing the Pharmacokinetics, Pharmacodynamics, and Safety of Recombinant Human InsulinCompletedNCT00358553Phase 1
- Efficacy of Albumin Dialysis to Treat Patients With Hepatic Encephalopathy Using The Molecular Adsorbent Recirculating System (MARS)CompletedNCT00287235Not applicable
- Safety Study to Evaluate Intracranial Pressure During High Frequency Chest Wall OscillationTerminatedNCT00279097Not applicable
- A Study to Evaluate the Efficacy and Safety of an Experimental Solution for Peritoneal DialysisCompletedNCT00214721Phase 3
- A Subjective Evaluation of Inflow Pain Associated With the Use of an Experimental Solution for Peritoneal DialysisCompletedNCT00214695Not applicable
- Performance and Safety of Bone Substitute MBCP-FS in Maxillary Sinus Lift ProceduresCompletedNCT00163605Phase 2/3
- Post-Marketing Surveillance of TISSUCOL for Hemostasis in Subjects Undergoing Vascular Reconstruction With Polytetrafluoroethylene (PTFE) ProsthesisCompletedNCT00163592
- Efficacy and Safety of Fibrin Sealant Vapor Heated Solvent/Detergent Treated (FS VH S/D) for Reduction of Lymphatic Leakage by Sealing Axillary Lymph Node Dissection SitesCompletedNCT00161980Phase 3
- Efficacy and Safety of Endoscopic Injection of Fibrin Sealant Versus Endoscopic Ligature for Bleeding Esophageal VaricesCompletedNCT00161915Phase 3
- Efficacy and Safety of Fibrin Sealant Vapor Heated Solvent/Detergent Treated (FS VH S/D) for Hemostasis in Subjects Undergoing Total Hip ReplacementCompletedNCT00161902Phase 3
- Safety and Efficacy Study of Fibrin Sealant (FS 4IU) for Skin Graft Fixation and Wound Healing in Subjects With Burn WoundsCompletedNCT00161759Phase 1/2
- Safety and Hemostatic Efficacy of Fibrin Sealant Vapor Heated, Solvent/Detergent Treated (FS VH S/D) Compared With Currently Licensed TISSEEL VH Fibrin Sealant in Subjects Undergoing Cardiac SurgeryCompletedNCT00161733Phase 3
- Safety and Efficacy Study of FS 4 IU VH S/D (Fibrin Sealant With 4IU/mL Thrombin, Vapor Heated, Solvent/Detergent Treated) to Adhere Split Thickness Skin Grafts and Improve Wound Healing in Burn PatientsCompletedNCT00157131Phase 3