# Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation

> **NCT05144126** · NA · UNKNOWN · sponsor: **CeraPedics, Inc** · enrollment: 300 (estimated)

## Conditions studied

- Degenerative Disc Disease

## Interventions

- **OTHER:** CT radioraphic assessment

## Key facts

- **NCT ID:** NCT05144126
- **Lead sponsor:** CeraPedics, Inc
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2022-01
- **Primary completion:** 2024-05
- **Final completion:** 2025-09
- **Target enrollment:** 300 (ESTIMATED)
- **Last updated:** 2021-12-03

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05144126

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05144126, "Safety, Radiological and Patient Reported Outcomes of i-FACTOR+ Matrix Bone Graft Device - A Canadian, Multicenter, Post-Market Clinical Investigation". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT05144126. Licensed CC0.

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