RecruitingPHASE1, PHASE2NCT06410001
CE-STAND: Cervical Epidural STimulation After Neurologic Damage
Studying Spinal cord injury
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
- University of Minnesota
- Principal Investigator
- Ann Parr, MD, PhDUniversity of Minnesota
- Intervention
- Epidural Spinal Cord Stimulation System(device)
- Enrollment
- 36 target
- Eligibility
- 22 years · All sexes
- Timeline
- 2026 – 2030
Study locations (1)
- University of Minnesota, Minneapolis, Minnesota, United States
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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