Medtronic: Chronic Pain trials

The registry lists 14 Chronic Pain studies with Medtronic as lead sponsor. 1 are open to participants now and 9 have results posted.

Phase 4 1No phase 13(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• Post Market Evaluation of Real World Outcomes and Durability to Support Implantable Inceptiv™ Spinal Cord Stimulation TherapyRecruitingNCT07507422
• Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (CMM) to CMM Alone in the Treatment of Intractable Back Pain Subjects Without Previous History of Lumbar Spine SurgeryCompletedNCT06442410Not applicableResults posted
• Electrically Evoked Compound Action Potentials Human Observation Medtronic Algorithm Comparison StudyCompletedNCT04765735Not applicableResults posted
• DTM (TM) Spinal Cord Stimulation (SCS) StudyCompletedNCT04601454Not applicableResults posted
• Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternative to Systemic Opioids for Chronic PainCompletedNCT03761277Phase 4Results posted
• Vectors Post Market: A Study to Assess Pain Relief Using Spinal Cord StimulationCompletedNCT03345472Not applicableResults posted
• Study of PM Modulation Therapy in Trial PhaseCompletedNCT03110601Not applicableResults posted
• Intrathecal Morphine Compared to Conventional Medical Management for Pain Control and Opioid-related Side EffectsTerminatedNCT01924182Not applicableResults posted
• Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Therapy (French SCS Registry)CompletedNCT01778426Results posted
• RestoreSensor StudyCompletedNCT01106404Not applicableResults posted
• Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)CompletedNCT06499220Not applicable
• Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal Cord Stimulation (SCS) Modalities for Chronic PainTerminatedNCT05775510
• Medtronic PSR TDD PMCFCompletedNCT04714385
• SynchroMed II Post-Approval StudyCompletedNCT00773019