# The Ailliance Post-Market Clinical Study

> **NCT05856370** · NA · RECRUITING · sponsor: **Medtronic Spinal and Biologics** · enrollment: 1000 (estimated)

## Conditions studied

- Spinal Deformity
- Spinal Degenerative Disorder
- Spinal Fusion Failure
- Spinal Trauma
- Spinal Tumor Case

## Interventions

- **DEVICE:** Follow-up schedule: pre-operative baseline up to 24-months post-procedure

## Key facts

- **NCT ID:** NCT05856370
- **Lead sponsor:** Medtronic Spinal and Biologics
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2023-05-01
- **Primary completion:** 2031-05
- **Final completion:** 2031-05
- **Target enrollment:** 1000 (ESTIMATED)
- **Last updated:** 2026-05-12

## Collaborators

- Medtronic Cardiac Rhythm and Heart Failure

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05856370

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05856370, "The Ailliance Post-Market Clinical Study". Retrieved via AI Analytics 2026-07-02 from https://api.ai-analytics.org/clinical/NCT05856370. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*