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Recruiting NCT07599904

NCT07599904 REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Ischemic Stroke (RECANOVA Registry)

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Clinical Trial Summary
NCT ID NCT07599904
Status Recruiting
Phase
Sponsor Medtronic Neurovascular Clinical Affairs
Condition Acute Ischemic Stroke
Study Type OBSERVATIONAL
Enrollment 1,500 participants
Start Date 2026-07-13
Primary Completion 2031-07

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Mechanical Thrombectomy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 1,500 participants in total. It began in 2026-07-13 with a primary completion date of 2031-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Post-Market Registry

Eligibility Criteria

Inclusion Criteria: 1. Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements. 2. Participant is treated or intended to be treated with a commercially available Medtronic Neurovascular device\* during treatment for acute ischemic stroke. 3. Participant is 18 years of age or older. Exclusion Criteria: 1. Participant who may be unable to complete follow-up within the registry. 2. Participant of child-bearing potential who is known to be pregnant or is breastfeeding or wishes to become pregnant during participation in the study. 3. Participant is currently enrolled in, or plans to enroll in, any concurrent drug/device study that may confound the study results based on Principal Investigator's discretion.

Contact & Investigator

Central Contact

Stephanie Salisbury

✉ rs.recanovaregistry@medtronic.com

📞 612-979-7251

Frequently Asked Questions

Who can join the NCT07599904 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Acute Ischemic Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07599904 currently recruiting?

Yes, NCT07599904 is actively recruiting participants. Contact the research team at rs.recanovaregistry@medtronic.com for enrollment information.

Where is the NCT07599904 trial being conducted?

This trial is being conducted at Flint, United States, Buffalo, United States, Houston, United States.

Who is sponsoring the NCT07599904 clinical trial?

NCT07599904 is sponsored by Medtronic Neurovascular Clinical Affairs. The trial plans to enroll 1,500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology