Clinical Trials Directory

Trials / Suspended

SuspendedNCT03871400

The NanoStrand Clinical Study

Comparison of Early Fusion Using a NanoMetalene® Implant Versus Both PEEK and Allograft Implants in Anterior Cervical Discectomy and Fusion (ACDF) With OsteoStrand™ Demineralized Bone Fibers

Status
Suspended
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
SeaSpine, Inc. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

A prospective, multi-center, randomized, self-controlled, single-blinded, clinical study evaluating the NanoMetalene implant as compared to the PEEK and allograft implants in ACDF for the treatment of cervical degenerative disc disease (DDD).

Detailed description

PEEK: Polyetheretherketone ACDF: Anterior cervical discectomy and fusion

Conditions

Interventions

TypeNameDescription
PROCEDUREAnterior cervical discectomy and fusionprimary, 2-level, contiguous

Timeline

Start date
2018-11-18
Primary completion
2020-06-15
Completion
2021-01-30
First posted
2019-03-12
Last updated
2020-10-19

Locations

11 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT03871400. Inclusion in this directory is not an endorsement.

The NanoStrand Clinical Study (NCT03871400) · Clinical Trials Directory