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The OsteoStrand Plus Deformity Study

NCT04629794 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2023-04-04

No results posted yet for this study

Summary

A clinical study evaluating outcomes for patients with spinal deformity.

Conditions

  • Spinal Fusion

Interventions

PROCEDURE

Posterolateral Lumbar Fusion with Demineralized Bone Fibers

Posterolateral Lumbar Fusion with Demimeralized Bone Fibers

PROCEDURE

Posterolateral Lumbar Fusion with Bone Morphogenic Protein

Posterolateral Lumbar Fusion with Bone Morphogenic Protein

Sponsors & Collaborators

  • SeaSpine, Inc.

    lead INDUSTRY

Principal Investigators

  • Michael Chang, MD · Sonoran Spine

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-05
Primary Completion
2024-03-31
Completion
2024-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04629794 on ClinicalTrials.gov