Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UC Davis UCSF
Dates
study started
completion around
Principal Investigator
by Kee Kim, MD (ucdavis)Aaron Clark, MD (ucsf)
Headshot of Aaron Clark
Aaron Clark

Description

Summary

The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s).

Subjects are enrolled and followed postoperatively to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.

Official Title

The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And Core spiNe produCt collEction

Keywords

Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case, Spinal Cord Neoplasms, Spinal Neoplasms, Follow-up schedule: pre-operative baseline up to 24-months post-procedure

Eligibility

Locations

  • University of California Davis Medical Center accepting new patients
    Sacramento California 95816 United States
  • University of California, San Francisco (UCSF) accepting new patients
    San Francisco California 94143 United States

Lead Scientists at University of California Health

  • Kee Kim, MD (ucdavis)
    Professor, Med: Neurological Surgery, School of Medicine. Authored (or co-authored) 89 research publications
  • Aaron Clark, MD (ucsf)
    Dr. Aaron Clark is a neurosurgeon specializing in minimally invasive outpatient procedures for lumbar and cervical herniated discs and stenosis, as well as minimally invasive lumbar fusion surgery. These procedures are associated with shorter recovery times and less postoperative pain than standard surgeries, and almost all patients can return home the same day.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Medtronic Spinal and Biologics
ID
NCT05856370
Study Type
Interventional
Participants
Expecting 1000 study participants
Last Updated