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Completed Not applicable Interventional Results available

Prospective, Multi-Center Clinical Outcomes Study Evaluating the chronOS Strip Combined With Bone Marrow Aspirate

ClinicalTrials.gov ID: NCT00943384

Public ClinicalTrials.gov record NCT00943384. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 2:24 AM EST

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Official title

Prospective, Multi-Center Clinical Outcomes Study Evaluating the chronOS Strip Combined With Bone Marrow Aspirate Plus Local Bone for Posterolateral Lumbar Interbody Fusion or Lumbosacral Interbody Fusion

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The chronOS Strip is a synthetic bone void filler manufactured from chronOS beta-tricalcium phosphate (β-TCP) granules and a resorbable polymer \[poly(lactide co-ε-caprolactone)\]. The chronOS Strip, combined with autogenous bone and/or bone marrow or autograft, is intended to be used in the spine for posterolateral fusion. The purpose of this prospective, multi-center clinical case series was to evaluate posterolateral fusion rates in a prospective series of patients with degenerative disc disease. The surgical procedure consisted of instrumented posterolateral fusion with interbody support. The chronOS Strip, combined with bone marrow aspirate and local bone, was applied to the posterolateral gutters.

Study identification

NCT ID
NCT00943384
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Synthes USA HQ, Inc.
Industry
Enrollment
104 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2009 (Type not available)
Primary completion
Oct 2013 (Actual)
Completion
Oct 2013 (Actual)
Last update posted
Nov 26, 2014

2009 – 2013

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
Hartford Hospital Hartford Connecticut 06102 —
Bay Area Neurosurgery Brandon Florida 33511 —
Atlanta Neurosurgical Associates Decatur Georgia 30033 —
Northwestern University Chicago Illinois 60611 —
University of Kansas Medical Center Kansas City Kansas 66160 —
The Boston Spine Group Newton Massachusetts 02458 —
Southern New York Neurosurgical Group Johnson City New York 13790 —
The Rothman Institute Philadelphia Pennsylvania 19020 —
University of Pennsylvania Philadelphia Pennsylvania 19107 —
UPMC Presbyterian Dept. of Neurosurgery Pittsburgh Pennsylvania 15213 —
Vanderbilt University Medical Center Department of Neurosurgery/Spine Research Nashville Tennessee 37232 —
Orthopaedic and Spine Center Newport News Virginia 23606 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00943384, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 26, 2014 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00943384 live on ClinicalTrials.gov.

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