Cervical Interbody Fusion Device Patient Registry

Status Active, not recruiting

Clinical Trial Summary

The registry has been designed as a prospective, observational program for patients undergoing anterior cervical discectomy and fusion (ACDF) procedures treated with TIDAL cervical interbody fusion device. The ultimate goal of the study is to aid in the development of treatment pathways and improved patient care. All patients who agree to participate in the registry will sign an informed consent form and subsequently be treated by their surgeon with the device in either an inpatient or outpatient facility.

Clinical Trial Description

The registry is design to collect data prospectively on patients undergoing spinal fusion using the TIDAL cervical interbody fusion device. Patients will be enrolled in the registry after reviewing the protocol with their health care provider and signing the informed consent. Data will be collected at recommended time points based on the standards of care of the participating sites. The registry will serve as a database in which retrospective analysis and exploratory analysis of specific research questions will be answered. Follow up visits will be defined by the treating physicians based on their standard practice. Typical clinical follow up schedules for patients undergoing this type of surgery are pre-operative and 12 months post-operative. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05114356
Study type	Observational [Patient Registry]
Source	Restor3D
Contact
Status	Active, not recruiting
Phase
Start date	November 8, 2021
Completion date	October 31, 2024

View Details

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