# Clinical Investigation of Clinical Safety and Performance of the SP-GRIPFLOW, Selective Cerebral Perfusion Catheter When Used for Cerebral Perfusion During Aortic Arch Repair

> **NCT05421130** · NA · UNKNOWN · sponsor: **Fuji Systems Corporation** · enrollment: 149 (estimated)

## Conditions studied

- Aortic Aneurysm
- Aortic Dissection
- Aortic Arch Aneurysm
- Aortic Arch; Aneurysm, Dissecting

## Interventions

- **DEVICE:** Selective Cerebral Perfusion Catheter

## Key facts

- **NCT ID:** NCT05421130
- **Lead sponsor:** Fuji Systems Corporation
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2022-05-02
- **Primary completion:** 2023-07-01
- **Final completion:** 2024-02-01
- **Target enrollment:** 149 (ESTIMATED)
- **Last updated:** 2023-07-11

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05421130

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05421130, "Clinical Investigation of Clinical Safety and Performance of the SP-GRIPFLOW, Selective Cerebral Perfusion Catheter When Used for Cerebral Perfusion During Aortic Arch Repair". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT05421130. Licensed CC0.

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