N/A N=30 Maternal Fetal Device Performance Singleton
Pregnancy
Primary: Success Rate Calculated Based on Collection of Fetal Heart Rate Data From Investigational Devices on Subjects Enrolled in Each Gestational Age Group — 85.01; 92.27…
Clinical Trial Search
Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.
N/A N=30 Electronic Device Implantation Through Remote Guidance
Telemedicine · Heart Failure · Defibrillators
Primary: Percentage of Participants With Interventional Procedures Successfully Completed — 10; 20 Participants
N/A N=1,509 Clinically Indicated Magnetic Resonance Imaging in Patients With Cardiac Devices
Arrhythmias, Cardiac
Primary: Device Malfunction — 24; 52 Participants
N/A N=24 Diagnostic Device Risk Management of Atrial Fibrillation and Heart Failure
Atrial Fibrillation · Heart Failure
Primary: Correlation of Heart Failure Risk Score (HFRS) With Heart Failure Events — 5; 2; 2; 7 participants
N/A N=12 Exploratory Investigation of Data Obtained From a Sensor Connected to an Intermittent Catheter
Compliance, Patient
Primary: Number of Participants With Readability of Pressure Sensor Measurements — 11 Participants
N/A N=83 Remote Device Interrogation In The Emergency Department
Heart Disease · Cardiovascular Disease · Heart Failure
Primary: Time to Interrogation — 25; 210 Minutes
N/A N=10 Monitoring Medication Adherence in Left Ventricular Assist Device Recipients
Heart Failure · Medication Compliance
Primary: System Performance - Positive Detection Accuracy — 80 percentage of ingestions
N/A N=86 Safety and Effectiveness Clinical Evaluation of Injectable Medical Devices Viscol
Aesthetic Dermatology
Primary: Performance at 1 Month Investigator Overall VISCOL Range — 77 Participants — p=<0.0001
N/A N=11 Implantable Microdevice for In Vivo Drug Sensitivity Testing in Patients With Early Stage, HER2-Positive or Triple Negative Breast Cancer
Breast Cancer
Primary: Number of Participants With Implantable Devices — 3; 5; 1; 2 Participants
Phase 3 N=20 Saizen® E-Device User Trial
Growth Disorders
Primary: Subjects' Overall Impression After Using E-Device — 0; 7; 13 subjects
N/A N=50 RF Surgical Sponge-Detecting System on the Function of Pacemakers and Implantable Cardioverter Defibrillators
Cardiomyopathy · Cardiac Arrhythmia · Heart Failure
Primary: Pacing Mode Changes Between Permanent Pacemakers (PPMs)/Implantable Cardiac Defibrillators (ICDs) Scanned With RF Assure — 29; 29; 8; 8 participants — p=1.0
N/A N=189 SJM MRI Diagnostic Imaging Registry (IDE)
Cardiac Arrhythmia
Primary: The Proportion of MRI Scans From Pacemakers or CRT-Ps Providing Sufficient Image Quality to Allow for a Diagnostic Interpretation. — 129 MRI Scans
N/A N=34 Usability Validation of Patient Monitoring Device for Pressure Injury Prevention and Fall Detection
Pressure Ulcer · Pressure Injury · Falls Injury
Primary: Usability Validation of Masimo Centroid System — 34 Participants
N/A N=262 Registry of Patients for MRI With Non-MRI Conditional Pacemakers and ICD Non-MRI Conditional Pacemakers and ICD
MRI Scans · Magnetic Resonance Imaging · Pacemaker
Primary: Number of Participants With Burning or Pulling Sensations in Chest/Device Pocket During MRI — 2 Participants
N/A N=20 Compass Device CVC Trial
Blood Pressure
Primary: Operator Satisfaction — 8 score on a scale
N/A N=118 Microcurrent Device (TIVIC Health)
Chronic Rhinosinusitis
Primary: Change in Pain Visual Analog Score After First Use of Device — 4.9; 5.6; 4.7; 4.8 score on a scale
N/A N=46 The EarLens Contact Hearing Device (CHD) Spectrum Study
Hearing Loss, Sensorineural
Primary: Change in Hearing Stability Using Unaided Air Conduction Thresholds. — -0.5 dB difference in Unaided Hearing
N/A N=240 Comparison Study in Adult Surgical Patients of 5 Airway Devices
Laryngoscopy · Intubation
Primary: Percentage Distribution of Cook's Modification of Cormack-Lehane's Grading System. Each Study Subject Will Receive a Grade of 1, 2A, 2B, 3A, 3B, or 4 in the…
Phase 3 N=10 PMP-300E (Smart Watch): Portable Monitoring Device Study
Obstructive Sleep Apnea
Primary: AHI — 19.2; 19.3 events/hour — p=>0.05
N/A N=161 Prospective Clinical Evaluation of BD NRFit™ Devices and Accessories.
Anesthesia · Analgesia
Primary: Primary Performance: Rate of Participants With Successful BD Spinal NRFit™ Needle Placement in the Subarachnoid Location — 100; 46; 146 Participants
N/A N=437 Reciprocating Medical Devices - a Study of a New Safety Device
Osteoarthritis · Rheumatoid Arthritis · Trauma
Primary: Pain Using VAS (Visual Analogue Pain Scale) — 5.2; 6.2 cm
N/A N=60 China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (ICD) [CN_MRI_ICD]
Tachycardia
Primary: Number of Participants With Freedom From Magnetic Resonance Imaging (MRI) Scan Related Complications — 14; 14; 15; 12 Participants
N/A N=59 Hospital Wearable Defibrillator Inpatient Study
In-Hospital Cardiac Arrest
Primary: Percentage of Time Rhythm Monitoring by the HWD1000 is Compromised Due to ECG Noise. — 0.53; 2.54 percentage of time worn
N/A N=388 Safety of Screening Procedures With Hand-held Metal Detectors Among Patients With Implanted Cardiac Rhythm Devices
Electromagnetic Interference
Primary: Electromagnetic Interference — 0 participants
N/A N=106 Wearable Technology to Reduce Risk of DVT and Increase Patient Compliance
Orthopedic Disorder
Primary: Compliance to Prescribed Use — 67.7; 83.3 percentage of prescribed use/24hr
N/A N=10 Demonstration of a New Device to Measure the Force of Delivering a Baby
Full Term Singleton Pregnancy
Primary: Force Exerted on a Fetus as the Delivery Occurs — 274.5 ounces
N/A N=58 BIONICS Israel Trial
Stenosis
Primary: Device Success in the Target Lesion as Determined by the Angiographic Core Laboratory — 58 Participants
N/A N=136 Ingenio Device Algorithm Study
Sinus Node Disease · AV Block · Heart Failure
Primary: Accuracy of Commanded Right Atrial Automatic Threshold (RAAT) — 100 percentage of accurate RAAT tests
N/A N=450 Prospective Observational Study of the Power PICC Family of Devices and Accessories
Peripherally Inserted Central Catheter
Primary: Primary Safety: Incidence of Symptomatic Venous Thrombosis in Patients With a Device From the BD PowerPICC Family Used for Both Short- and Long-term Venous Access. — 1.6…
N/A N=664 MarginProbe, a Device for Intraoperative Assessment of Margin Status in Breast Conservation Surgery
Breast Cancer
Primary: The Primary Effectiveness Endpoint is a Measure of Intraoperative Success in Addressing Positive Margins as Detected by Permanent Pathology)by Additional Oriented Tissue…