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A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

NCT01494428 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2023-05-17

No results posted yet for this study

Summary

The purpose of this pilot clinical trial is to evaluate the device design as a method of facilitating spinal fusion.

Conditions

  • Degenerative Disc Disease

Interventions

DEVICE

rhBMP-2/ACS/allograft bone dowel

The rhBMP-2/ACS will be used in conjunction with an allograft bone dowel.

DEVICE

Autogenous bone/allograft bone dowel

An allograft bone dowel contains autogenous bone taken from the patient's iliac crest.

Sponsors & Collaborators

  • Medtronic Spinal and Biologics

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1998-04-30
Primary Completion
2004-02-29
Completion
2004-02-29

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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 NCT01494428 on ClinicalTrials.gov