Medtronic - MITG
Medtronic - MITG sponsors 119 registered US clinical trials on ClinicalTrials.gov, 5 of them currently recruiting, and 99 completed. 5 of these trials are in Phase 3-4 (later-stage) and 5 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Hypoxia, with 3 trials.
Trial Pipeline
119 total, page 1 of 3
Solv Multi-Pass Hemodialysis System In-Center Clinical Study
NCT07216885
Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in Left-sided Colon, Sigmoid, and Rectal Resections
NCT07351071
Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace Gynecology)
NCT07120945
AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Undergoing Ventral Hernia Repair
NCT06710795
Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal Upper Gastrointestinal Bleeding
NCT06188585
Accuracy Verification of the INVOS PM7100
NCT07166341
Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia
NCT06449378
Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable Hernia Repair)
NCT06445504
Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Urologic Surgery (Expand URO)
NCT05696444
Prospective, Multi-center, Single-arm, Observational Study. US FDA 522 Pediatric Post Market Surveillance Study.
NCT04608149
Nellcor™ Abbreviated Sensor Additional Data Collection
NCT07201961
Philips FAST Evaluation
NCT06860230
OM2 Low Saturation Verification
NCT06661889
Accuracy Performance Verification of the INVOS™ PM7100 System in Adults
NCT06581835
Pulse Oximetry Performance Comparison in Newborns
NCT06637917
Perfusion Index Parameter
NCT06586918
OM2 Motion Verification Study
NCT06415786
OM2 Abbreviated Sensor Verification
NCT06415799
Accuracy Performance Verification of the INVOS™ System in Pediatrics
NCT05962905
N600X Low Saturation Accuracy Validation
NCT05532670
Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patients
NCT04810481
SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor
NCT04811963
Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhalational Anesthetics in Healthy Volunteers (OLIVER)
NCT04602546
SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion Study
NCT04559763
Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil in Healthy Volunteers (SONORA)
NCT04466384
A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapling System.
NCT03515811
Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Developments (SODA)
NCT03771508
A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy
NCT03266094
superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Technology
NCT03585959
Trending of Respiratory Rate Using the Nellcor™ Bedside Respiratory Patient Monitoring System
NCT03593603
Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair
NCT03495154
A Comparison of Capnography Sampling Lines
NCT03554629
Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks
NCT03526341
Clinical Study Comparing PillCam® Crohn's Capsule Endoscopy to Ileocolonoscopy (IC) Plus MRE for Detection of Active CD in the Small Bowel and Colon in Subjects With Known CD and Mucosal Disease.
NCT03241368
Validation of Next Generation Cerebral and Tissue Oximeter
NCT03128372
PRediction of Opioid-induced Respiratory Depression In Patients Monitored by capnoGraphY
NCT02811302
Surveillance Monitoring as an Alternative to Telemetry
NCT03039738
Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM) and Utility of IPI.
NCT03050983
A Study of BiZact™ on Adults Undergoing Tonsillectomy
NCT02876575
Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in the Identification of Colonic Polyps in a Screening Population.
NCT02754661
Impact of Neuromonitoring During Cardiac Procedures
NCT02681731
Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit)
NCT02707003
Performance Assessment of a Remote Patient Monitoring Device
NCT02570906
Cytosponge Adequacy Study Evaluation II
NCT02395471
Optimization of the Bowel Preparation Regimen for the PillCam® COLON 2 Capsule Endoscopy Procedure
NCT02481219
NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electromagnetic Navigation Bronchoscopy™
NCT02410837
Case Series to Evaluate the Identification of Anatomical Markers Using the KANGAROO™ Feeding Tube
NCT02430571
The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (EMPRESS)
NCT02323854
A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Pylorus Sparing (SIPS) Procedure
NCT02275208
Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Samples During Motion
NCT02247765
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 3 |
| Phase 2 | 2 |
| Phase 3 | 1 |
| Phase 4 | 4 |
What the Pipeline for Medtronic - MITG Shows
According to the ClinicalTrials.gov registry, Medtronic - MITG is linked to 119 US clinical trials across every stage of research activity. Of those, 5 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 99 are already marked complete, representing roughly 83% of the total.
The phase mix for Medtronic - MITG reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 5 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Medtronic - MITG is Hypoxia with 3 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.