Viewing Study NCT06559735


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Ignite Modification Date: 2025-12-25 @ 8:12 PM
Study NCT ID: NCT06559735
Status: RECRUITING
Last Update Posted: 2024-08-19
First Post: 2024-08-12
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Local Cerebral Oxygenation in Chronic Pain Patients Utilizing Spinal Cord Stimulation
Sponsor: CereVu Medical, Inc.
Organization:

Study Overview

Official Title: A Prospective, Observational Study Examining Local Cerebral Oxygenation in Chronic Pain Patients Utilizing Spinal Cord Stimulation
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary objective of the study is to determine changes in cerebral nociceptive hemodynamic response (blood oxygenation/flow) before, during and following spinal cord stimulation (SCS). Objective measurements of cerebral nociceptive hemodynamic responses will be obtained with the CereVu sensor and ROPA system and will be analyzed offline and compared against subjective measures of pain. Proprietary analysis algorithms will be incorporated and developed to understand how the objective measurements correlate with subject reported pain levels
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: True
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: