# Post-Market Surveillance Study to Evaluate the Long-Term Safety and Effectiveness of the LVIS Device

> **NCT05453240** · — · ENROLLING_BY_INVITATION · sponsor: **Microvention-Terumo, Inc.** · enrollment: 250 (estimated)

## Conditions studied

- Intracranial Aneurysms

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT05453240
- **Lead sponsor:** Microvention-Terumo, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2020-11-17
- **Primary completion:** 2025-10-01
- **Final completion:** 2026-01-01
- **Target enrollment:** 250 (ESTIMATED)
- **Last updated:** 2025-06-17


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05453240

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05453240, "Post-Market Surveillance Study to Evaluate the Long-Term Safety and Effectiveness of the LVIS Device". Retrieved via AI Analytics 2026-06-30 from https://api.ai-analytics.org/clinical/NCT05453240. Licensed CC0.

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