MedtronicNeuro
MedtronicNeuro sponsors 51 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 36 completed. 8 of these trials are in Phase 3-4 (later-stage) and 3 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Chronic Pain, with 3 trials.
Trial Pipeline
51 total, page 1 of 2
Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial Device
NCT07456865
Pelvic Health Electrically Evoked Recording (PEER) 2 Study
NCT05200923
Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study (EPAS)
NCT03900468
Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal Cord Stimulation (SCS) Modalities for Chronic Pain
NCT05775510
Evaluation of Implantable Tibial Neuromodulation Pivotal Study (TITAN 2)
NCT05226286
Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study
NCT04873271
Electrically Evoked Compound Action Potentials Human Observation Medtronic Algorithm Comparison Study
NCT04765735
Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease
NCT04547712
DTM (TM) Spinal Cord Stimulation (SCS) Study
NCT04601454
InterStim Micro Post Market Clinical Follow-up Study (ELITE)
NCT04506866
InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study
NCT04016324
Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)
NCT06499220
Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternative to Systemic Opioids for Chronic Pain
NCT03761277
SCS Research Study
NCT03763708
LFP Beta aDBS Feasibility Study
NCT03446833
Visualase Visualization Database (VIVID-1)
NCT03489187
InterStim® Amplitude Study
NCT03335761
Vectors Post Market: A Study to Assess Pain Relief Using Spinal Cord Stimulation
NCT03345472
Spinal Cord Stimulation (SCS) Dosing Study
NCT03284411
OsteoCool Tumor Ablation Post-Market Study
NCT03249584
Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate)
NCT02844465
PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial Neuromodulation System in Patients With OAB
NCT02857816
OPTIONS Spinal Cord Stimulation Programming Parameters
NCT02503787
Intrathecal Morphine Compared to Conventional Medical Management for Pain Control and Opioid-related Side Effects
NCT01924182
InterStim® Sacral Nerve Modulation Cycling Study
NCT01957137
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
NCT01818297
Spinal Cord Stimulation for Predominant Low Back Pain
NCT01697358
Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Management Software Feasibility Study
NCT01750242
Epilepsy Motion Sensing
NCT01850498
Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who Have Problems With Intrathecal Drug Delivery
NCT01117090
RestoreSensor Study
NCT01106404
InterStim Therapy Programming Study
NCT01009333
SISTERS: Spasticity In Stroke Study - Randomized Study
NCT01032239
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
NCT00998660
Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression
NCT00837486
Spinal Cord Stimulation Research Study
NCT00768872
Spinal Cord Stimulation Research Study
NCT00737581
A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Treatment of Chronic Pain
NCT00414466
A Cost Analysis of Interstim Therapy
NCT00200031
Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Diabetes
NCT00200018
Restore Claims Characterization Study
NCT00200122
Patient Registry to Study the Tined Lead Used With the InterStim System For Urinary Control
NCT00225966
Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache.
NCT00200109
Study of Weight Loss Using Gastric Stimulation in Obese Patients
NCT00200083
Implantable Systems Performance Registry
NCT00959296
Neurostimulation to Treat Refractory Angina Pectoris Pain
NCT00200070
An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS With Gastroesophageal Reflux Disease (GERD)
NCT00200044
Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis)
NCT00157755
Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence
NCT00200057
Sacral Nerve Stimulation for Anal Incontinence and Bowel Control
NCT00200005
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 1 |
| Phase 2 | 2 |
| Phase 3 | 1 |
| Phase 4 | 7 |
Therapeutic Areas
What the Pipeline for MedtronicNeuro Shows
According to the ClinicalTrials.gov registry, MedtronicNeuro is linked to 51 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 36 are already marked complete, representing roughly 71% of the total.
The phase mix for MedtronicNeuro reports 8 late-stage studies (Phase 3 and Phase 4 combined) and 3 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for MedtronicNeuro is Chronic Pain 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.