Efficacy Study of NuCel® in Patients Undergoing Fusion of the Lumbar Spine

Status Completed

Clinical Trial Summary

The purpose of this study is to determine whether NuCel is effective in promoting spinal fusion in degenerative disease of the lumbar spine.

Clinical Trial Description

The study is a prospective, single center clinical trial to establish the efficacy of NuCel, a minimally manipulated allograft tissue, for use in lumbar interbody and intertransverse fusion procedures. Subjects will undergo standard interbody fusion surgery as per the signed informed consent with NuCel and autograft bone. Patients will be evaluated postoperatively at 6 weeks, 3 months, 6 months, 1 year, and 2 years (if required). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02023372
Study type	Interventional
Source	NuTech Medical, Inc
Contact
Status	Completed
Phase	N/A
Start date	December 2013
Completion date	August 16, 2019

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT06290908` - RPE-P/TLIF for Lumbar Spinal Stenosis With Instability
Withdrawn	`NCT03223701` - Efficacy of Using Solum IV and BMC With GFC in TLIF	Phase 4
Recruiting	`NCT03883022` - Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery	N/A
Completed	`NCT02902380` - The Effect of Dexmedetomidine on Neuroendocrine Stress Hormone Release and Heart Rate Variability in Patients Undergoing Major Spinal Surgery	N/A
Not yet recruiting	`NCT06024785` - Vertebropexy - Randomized-controlled Trial	N/A
Not yet recruiting	`NCT06000319` - Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion
Completed	`NCT02558621` - New Robotic Assistance System for Spinal Fusion Surgery	N/A
Completed	`NCT02454400` - Pre-surgery Physiotherapy for Patients With Specific Low Back Pain	N/A
Completed	`NCT01377623` - Pilot Study on the Effect of Dexmedetomidine on Inflammatory Responses in Patients Undergoing Lumbar Spinal Fusion	N/A
Completed	`NCT00996073` - Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody Fusion	Phase 2
Terminated	`NCT00974623` - Bone Graft Materials Observational Registry	N/A
Completed	`NCT00022776` - Surgical Versus Nonsurgical Treatment for Spinal Stenosis	Phase 3
Completed	`NCT00320619` - Epsilon-Aminocaproaic Acid to Reduce the Need for Blood Transfusions During and Following Spine Surgery	N/A
Completed	`NCT06060821` - Validity and Reliability of the 2-minute Step Test in Patients With Lumbar Spinal Stenosis
Recruiting	`NCT04552145` - Physical Therapy vs Surgical Decompression for Lumbar Spinal Stenosis	N/A
Active, not recruiting	`NCT04379921` - Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using the Apple Watch	N/A
Withdrawn	`NCT04315090` - Post-surgical Outcomes Measure Using the ERAS Protocol for Posterior Cervical Decompression and Fusion
Completed	`NCT04591249` - Physical Activity Intervention for Patients Following Lumbar Spine Surgery	N/A
Recruiting	`NCT04601363` - Personalized Spine Study Group (PSSG) Registry
Completed	`NCT04193488` - Mid-Transverse Process to Pleural (MTP) Block and Erector Spinal Plan (ESP) Block in Spinal Surgery	N/A