Health Trials

Safety, Performance and Usability of BALT Medical Devices: The EVIDENCE Post Marketing Clinical Follow-up Platform

ConditionsIntracranial AneurysmBrain Arterial DiseaseAcute Ischemic StrokePeripheral Vascular DiseasesAVM - Cerebral Arteriovenous MalformationAVMFistulas Arteriovenous
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2+
SponsorBalt Extrusion

About this trial

BALT has designed an electronic platform to continue collecting clinical data as part of the post-marketing clinical follow-up of its devices.

This platform is purely exploratory, without hierarchical order of the objectives and associated outcomes.

Eligibility criteria

Qualifiers

Provision of a signed, written and dated informed consent or non-opposition (where applicable)

Disqualifiers

Device(s) used in multiple procedures (two, or more, pathologies treated during the same procedure)

Contra-indications of each device as described in the instructions for use.

Trial design

Treatments tested in this trial

  • BALT medical devices

Treatment groups

10,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

Balt Extrusion

Lead sponsor

Source ClinicalTrials.gov