# Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes

> **NCT07222787** · NA · RECRUITING · sponsor: **Providence Medical Technology, Inc.** · enrollment: 250 (estimated)

## Conditions studied

- Radiculopathy Lumbar
- Degenerative Lumbar Disc Disease

## Interventions

- **DEVICE:** Supplemental Posterior Fusion with Study Device
- **DEVICE:** Supplemental Posterior Fusion with Standard Technique

## Key facts

- **NCT ID:** NCT07222787
- **Lead sponsor:** Providence Medical Technology, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-12-01
- **Primary completion:** 2028-07-01
- **Final completion:** 2029-07-01
- **Target enrollment:** 250 (ESTIMATED)
- **Last updated:** 2026-05-01


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07222787

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07222787, "Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT07222787. Licensed CC0.

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