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CAPTURER PMCF Study ( rEPIC04D )

CAPTURER PMCF Post-Market Clinical Follow-up Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05292079
Acronym
rEPIC04D
Enrollment
86
Registered
2022-03-23
Start date
2022-09-29
Completion date
2023-12-27
Last updated
2024-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease (CAD), Ischemic Heart Disease

Keywords

MDR (Medical Device Regulations), PMCF (Post-Market Clinical Follow-up), Thrombus extraction catheter

Brief summary

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

Detailed description

The objective of this multicenter, prospective, non-randomized, post-market clinical follow-up (PMCF) study is to confirm and support the clinical safety and performance of the CAPTURER in a NON-SELECTED, Real World population under daily clinical practice when used as intended by the manufacturer to meet EU Medical Device regulation requirements for post-market clinical follow-up.

Interventions

DEVICECAPTURER

Patients in whom treatment with (CAPTURER) has been attempted

Sponsors

Fundación EPIC
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient treated with CAPTURER according to routine hospital practice and following instructions for use * Informed consent signed

Exclusion criteria

* Not meet inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Safety Endpoint. Freedom from Target Lesion Failure30 daysFreedom from TARGET LESION FAILURE (TLF), composite end point of cardiac death, myocardial infarction, stroke and and new Target Lesion Revascularization (TLR)

Secondary

MeasureTime frameDescription
Freedom from Device ruptureDuring percutaneous coronary intervention (PCI)Freedom from Device rupture
Freedom from KinkingDuring PCIFreedom from Kinking
Freedom from Complicated withdrawalDuring PCIFreedom from Complicated withdrawal
Efficacy Endpoint. Freedom from Target Lesion Failure30 daysFreedom from TARGET LESION FAILURE (TLF), composite endpoint of cardiac death, myocardial infarction (MI) and and new Target Lesion Revascularization (TLR)
Freedom from Coronary dissection >CDuring PCIFreedom from Coronary dissection \>C
Freedom from No reflowDuring PCIFreedom from No reflow
Freedom from Coronary thrombosisDuring PCIFreedom from Coronary thrombosis
Freedom from Coronary perforationDuring PCIFreedom from Coronary perforation

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026