Follows patients treated with BALT devices for brain artery conditions
Collects follow-up data on BALT devices used for brain artery disease.
Plain-language title generated from the registry record
Registry title: Safety, Performance and Usability of BALT Medical Devices: The EVIDENCE Post Marketing Clinical Follow-up Platform
Key facts
- Where
- Halle, GermanySee the site
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
This platform collects follow-up data on people treated with BALT medical devices for blood vessel conditions in the brain or body. The record lists only consent as an inclusion rule.
- Age
- 2 years and older
- Sex
- All sexes can join
Main reasons for not taking part
- Device used in several procedures (two or more diseases treated in the same procedure)
- Contra-indications of each device listed in its instructions for use
Read by machine on 12 November 2026.
Where in Germany
- HalleHalle, GermanyContact: zhanna SvatkoTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Balt Extrusion
- Trial code
- NCT04927156
- Record updated
- 18 September 2025
- Original description
BALT has designed an electronic platform to continue collecting clinical data as part of the post-marketing clinical follow-up of its devices.Read full original descriptionShow less
Safety, Performance and Usability of BALT Medical Devices: The EVIDENCE Post Marketing Clinical Follow-up Platform. An International, Multicenter, Prospective, and Retrospective Data Collection
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.
Inclusion: Provision of a signed, written and dated informed consent or non-opposition (where applicable).
Exclusion: 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.