# Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion

> **NCT06744907** · PHASE4 · RECRUITING · sponsor: **Akron Children's Hospital** · enrollment: 60 (estimated)

## Conditions studied

- Spinal Fusion

## Interventions

- **BIOLOGICAL:** 10% Povidone-Iodine Arm
- **PROCEDURE:** Saline Arm

## Key facts

- **NCT ID:** NCT06744907
- **Lead sponsor:** Akron Children's Hospital
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-01-03
- **Primary completion:** 2025-11
- **Final completion:** 2026-11
- **Target enrollment:** 60 (ESTIMATED)
- **Last updated:** 2025-01-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06744907

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06744907, "Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion". Retrieved via AI Analytics 2026-06-24 from https://api.ai-analytics.org/clinical/NCT06744907. Licensed CC0.

---

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