TerminatedNot applicableNCT03786432
Prospective Study of Fusion Rates Using Spira-C Device for Anterior Cervical Discectomy and Fusion Surgery
Studying Paraneoplastic neurologic syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Corewell Health East
- Principal Investigator
- Jad G Khalil, MD, MSW, LCSWCorewell Health East
- Intervention
- Spira-C Interbody Device(device)
- Enrollment
- 13 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2022
Study locations (1)
- William Beaumont Hospital, Royal Oak, Michigan, United States
Collaborators
Camber Spine Technologies
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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