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RECRUITING
NCT06631157
Essential Pro Study ( rEPIC04E-HK )
Sponsor: Fundación EPIC
View on ClinicalTrials.gov
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.
Official title: Essential Pro Post-Market Clinical Follow-up Study
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2025-05-15
Completion Date
2026-11-01
Last Updated
2026-02-17
Healthy Volunteers
No
Interventions
DEVICE
Essential pro
Patients in whom treatment with (Essential Pro) has been attempted
Locations (1)
Princess Margaret Hospital
Lai Chi Kok, Hong Kong