Essential Pro Study ( rEPIC04E-HK )
Essential Pro Post-Market Clinical Follow-up Study
Fundación EPIC
100 participants
May 15, 2025
OBSERVATIONAL
Conditions
Summary
Single center, prospective, non-randomized, post-market clinical follow-up (PMCF) study to confirm and support the clinical safety and performance of Essential Pro to meet EU Medical Device regulation (MDR) requirements in all the CONSECUTIVE patients treated with Essential Pro.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Patients in whom treatment with (Essential Pro) has been attempted
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06631157