Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Product Surveillance Registry

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

Participants needed: 100,000
Trial details
Biological sex: AllType: ObservationalSponsor: MedtronicUpdated: Jun 17, 2026Locations: 395
Eligibility criteria

Patient or legally authorized representative provides written authorization and/... [+2]

Patient who is, or will be, inaccessible for follow-up [+2]

Status: Recruiting

Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products

The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: MedtronicUpdated: May 7, 2026Locations: 320
Eligibility criteria

Subject is indicated for implant or within 30 days post-implant of at least one... [+5]

Status: Recruiting

Post Market Evaluation of Real World Outcomes and Durability to Support Implantable Inceptiv™ Spinal Cord Stimulation Therapy

The PERSIST study is being conducted within Medtronic's active post-market surveillance platform, the Product Surveillance Registry (PSR). The purpose of PERSIST is to generate long-term evidence for the Inceptiv™ Spinal Cord Stimulation therapy.

Participants needed: 970
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: MedtronicUpdated: May 4, 2026Locations: 3Duration: 5 Years
Eligibility criteria

18 years of age or older [+8]

Has any existing or is planning to have a new active implantable neuromodulation... [+36]

Status: Recruiting

Propel Drug-Eluting Sinus Implant Family IBUKI Cohort

To confirm clinical safety and performance for the PROPEL family of products when used according to IFUs and standard of care in Japan.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: MedtronicUpdated: Apr 23, 2026Locations: 1Duration: 6 Months
Eligibility criteria

Patient or legally authorized representative (LAR) provides authorization and/or... [+6]

Patient has clinical evidence of disease or a condition expected to compromise s... [+4]