# Evaluation of Plenum® Tissue Ortho to Prevent Epidural Fibrosis and Post-laminectomy Syndrome.

> **NCT05776628** · NA · UNKNOWN · sponsor: **M3 Health** · enrollment: 36 (estimated)

## Conditions studied

- Herniated Disk Lumbar

## Interventions

- **DEVICE:** Plenum® Tissue ortho membrane (polydioxanone membrane)

## Key facts

- **NCT ID:** NCT05776628
- **Lead sponsor:** M3 Health
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2024-04
- **Primary completion:** 2024-10
- **Final completion:** 2025-04
- **Target enrollment:** 36 (ESTIMATED)
- **Last updated:** 2024-03-12

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05776628

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05776628, "Evaluation of Plenum® Tissue Ortho to Prevent Epidural Fibrosis and Post-laminectomy Syndrome.". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT05776628. Licensed CC0.

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