Initial clinical experience with the Artisse-Device

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00039147

Enrollment

Registered

2026-01-29

Start date

2026-01-14

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

I67.1

Interventions

Group 1: Retrospective analysis of all patients treated for a cerebral aneurysm using Artisse between 1/2024 and 5/2025.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Treatment with Artisse

Exclusion criteria

Exclusion criteria: The patient refused the use of their data for research purposes.

Design outcomes

Primary

Measure	Time frame
Degree of aneurysma occlusion	—

Secondary

Measure	Time frame
Are there clinical or morphological factors associated with sizing deviations between simulated and manual sizing?	—

Countries

Germany

Contacts

Public ContactTobias Boppel

UKSH

tobias.boppel@uksh.de+49 451 50017201

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026