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Xperience Pro PMCF Study

NCT05292144 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2023-05-30

No results posted yet for this study

Summary

Multicenter, prospective, non-randomized, post-market clinical follow-up (PMCF) study to confirm and support the clinical safety and performance of Xperience Pro to meet EU Medical Device regulation (MDR) requirements in all the CONSECUTIVE patients treated with Xperience Pro .

Conditions

  • Coronary Artery Disease (CAD)
  • Ischemic Heart Disease

Interventions

DEVICE

Xperience Pro

Patients in whom treatment with (Xperience Pro) has been attempted

Sponsors & Collaborators

  • Fundación EPIC

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-10-26
Primary Completion
2023-04-26
Completion
2023-05-05

Countries

  • Spain

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 NCT05292144 on ClinicalTrials.gov