MedtronicNeuro

51 total trials 2 currently recruiting 36 completed

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

RECRUITING NA

Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial Device

NCT07456865

RECRUITING NA

Pelvic Health Electrically Evoked Recording (PEER) 2 Study

NCT05200923

ACTIVE NOT RECRUITING NA

Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study (EPAS)

NCT03900468

TERMINATED

Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal Cord Stimulation (SCS) Modalities for Chronic Pain

NCT05775510

COMPLETED NA

Evaluation of Implantable Tibial Neuromodulation Pivotal Study (TITAN 2)

NCT05226286

COMPLETED NA

Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study

NCT04873271

COMPLETED NA

Electrically Evoked Compound Action Potentials Human Observation Medtronic Algorithm Comparison Study

NCT04765735

COMPLETED NA

Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease

NCT04547712

COMPLETED NA

DTM (TM) Spinal Cord Stimulation (SCS) Study

NCT04601454

TERMINATED NA

InterStim Micro Post Market Clinical Follow-up Study (ELITE)

NCT04506866

COMPLETED NA

InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study

NCT04016324

COMPLETED NA

Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)

NCT06499220

COMPLETED Phase 4

Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternative to Systemic Opioids for Chronic Pain

NCT03761277

TERMINATED NA

SCS Research Study

NCT03763708

TERMINATED NA

LFP Beta aDBS Feasibility Study

NCT03446833

COMPLETED

Visualase Visualization Database (VIVID-1)

NCT03489187

COMPLETED NA

InterStim® Amplitude Study

NCT03335761

COMPLETED NA

Vectors Post Market: A Study to Assess Pain Relief Using Spinal Cord Stimulation

NCT03345472

COMPLETED Phase 4

Spinal Cord Stimulation (SCS) Dosing Study

NCT03284411

COMPLETED NA

OsteoCool Tumor Ablation Post-Market Study

NCT03249584

COMPLETED NA

Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate)

NCT02844465

COMPLETED NA

PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial Neuromodulation System in Patients With OAB

NCT02857816

COMPLETED NA

OPTIONS Spinal Cord Stimulation Programming Parameters

NCT02503787

TERMINATED NA

Intrathecal Morphine Compared to Conventional Medical Management for Pain Control and Opioid-related Side Effects

NCT01924182

COMPLETED NA

InterStim® Sacral Nerve Modulation Cycling Study

NCT01957137

TERMINATED NA

Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients

NCT01818297

COMPLETED Phase 4

Spinal Cord Stimulation for Predominant Low Back Pain

NCT01697358

COMPLETED

Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Management Software Feasibility Study

NCT01750242

COMPLETED

Epilepsy Motion Sensing

NCT01850498

COMPLETED

Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who Have Problems With Intrathecal Drug Delivery

NCT01117090

COMPLETED NA

RestoreSensor Study

NCT01106404

COMPLETED NA

InterStim Therapy Programming Study

NCT01009333

COMPLETED Phase 4

SISTERS: Spasticity In Stroke Study - Randomized Study

NCT01032239

COMPLETED Phase 4

RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)

NCT00998660

COMPLETED Phase 2

Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression

NCT00837486

COMPLETED

Spinal Cord Stimulation Research Study

NCT00768872

COMPLETED

Spinal Cord Stimulation Research Study

NCT00737581

TERMINATED Phase 2

A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Treatment of Chronic Pain

NCT00414466

COMPLETED

A Cost Analysis of Interstim Therapy

NCT00200031

COMPLETED NA

Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Diabetes

NCT00200018

COMPLETED Phase 4

Restore Claims Characterization Study

NCT00200122

TERMINATED NA

Patient Registry to Study the Tined Lead Used With the InterStim System For Urinary Control

NCT00225966

COMPLETED Phase 1

Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache.

NCT00200109

COMPLETED NA

Study of Weight Loss Using Gastric Stimulation in Obese Patients

NCT00200083

COMPLETED

Implantable Systems Performance Registry

NCT00959296

TERMINATED Phase 3

Neurostimulation to Treat Refractory Angina Pectoris Pain

NCT00200070

TERMINATED NA

An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS With Gastroesophageal Reflux Disease (GERD)

NCT00200044

TERMINATED NA

Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis)

NCT00157755

COMPLETED NA

Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence

NCT00200057

COMPLETED Phase 4

Sacral Nerve Stimulation for Anal Incontinence and Bowel Control

NCT00200005

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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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.