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Safety, Performance of CEREGLIDE 92 Intermediate Catheter in Treatment of Acute Ischemic Stroke - Trial NCT06386289

Access comprehensive clinical trial information for NCT06386289 through Pure Global AI's free database. This phase not specified trial is sponsored by Cerenovus, Part of DePuy Synthes Products, Inc. and is currently Not yet recruiting. The study focuses on Acute Ischemic Stroke. Target enrollment is 172 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT06386289
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Safety, Performance of CEREGLIDE 92 Intermediate Catheter in Treatment of Acute Ischemic Stroke
Safety, Performance and Lesion Evaluation of Neurothrombectomy Using CEREGLIDE 92 Intermediate Catheter: A Prospective Multi-Center Single-Arm IDE Trial (SPLENDID)

Study Focus

Acute Ischemic Stroke

Cereglide 92

Interventional

device

Sponsor & Location

Cerenovus, Part of DePuy Synthes Products, Inc.

Iowa City,Edison,Valhalla,Nashville,Salt Lake City,Morgantown, United States of America

Timeline & Enrollment

N/A

Sep 01, 2024

Jun 30, 2026

172 participants

Primary Outcome

First pass reperfusion

Summary

The device is indicated for use in the revascularization of patients with acute ischemic
 stroke secondary to intracranial large vessel occlusive disease

ICD-10 Classifications

Stroke, not specified as haemorrhage or infarction
Sequelae of stroke, not specified as haemorrhage or infarction
Cerebral infarction
Cerebral infarction, unspecified
Transient cerebral ischaemic attack, unspecified

Data Source

ClinicalTrials.gov

NCT06386289

Device Trial