Symplicity China Study

NCT07081243 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-11-17

No results posted yet for this study

Summary

The Symplicity China study will evaluate the real-world long-term safety, efficacy, and durability of the Symplicity Spyral system in a population of approximately 500 renal denervation treated subjects with up to 36 months of follow up.

Conditions

  • Resistant Hypertension

Interventions

DEVICE

Symplicity Spyral Renal Denervation System

Symplicity Renal Denervation

Sponsors & Collaborators

  • Medtronic Vascular

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-11
Primary Completion
2028-06-30
Completion
2031-12-30
FDA Device
Yes

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07081243 on ClinicalTrials.gov