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Spondylolisthesis, Grade 1 clinical trials

View clinical trials related to Spondylolisthesis, Grade 1.

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NCT ID: NCT06415110 Enrolling by invitation - Clinical trials for Spondylolisthesis, Grade 1

A Prospective Analysis of the Efficacy of Allosync Expand and Autograft Bone Graft in Open Lumbar Spinal Fusion

Start date: May 2024
Phase:
Study type: Observational

The purpose of this study is to assess the radiographic and clinical outcomes of spinal fusion following use of Allosync Expand and autograft bone graft.

NCT ID: NCT03928041 Completed - Clinical trials for Spondylolisthesis, Grade 1

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced Interbody Cages in the Lumbar Spine

Start date: June 27, 2019
Phase: N/A
Study type: Interventional

The purpose of this trial is to collect clinical outcomes including radiographic and CT outcomes in patients who undergo interbody spinal fusion using the EVOS Lumbar Interbody System.

NCT ID: NCT03381677 Suspended - Clinical trials for Lumbar Spinal Stenosis

Pedicle Osteotomy for Stenosis Trial

POST
Start date: October 26, 2017
Phase: N/A
Study type: Interventional

This is a pivotal Randomized Clinical trial to compare the safety and effectiveness of the Pedicle Lengthening Osteotomy Procedure with implantation of the Altum® Device to open surgical decompression and Transforaminal Lumbar Interbody Fusion (TLIF) in patients with symptomatic, one or two level lumbar spinal stenosis (LSS) and one level grade I degenerative spondylolisthesis requiring surgical treatment.

NCT ID: NCT02704689 Terminated - Clinical trials for Degenerative Disc Disease

AccuLIF® PROSPECTIVE PATIENT OUTCOMES STUDY

APROPOS
Start date: June 8, 2016
Phase: N/A
Study type: Interventional

This is a post-market clinical study of the AccuLIF expandable transforaminal lumbar interbody fusion (TLIF) cage in patients requiring surgery for degenerative disc disease (DDD) with up to Grade I spondylolisthesis or retrolisthesis, at one or two levels, between L2 and S1.

NCT ID: NCT01944345 Completed - Clinical trials for Intervertebral Disc Degeneration

Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device

Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

The registry has been designed as a prospective, observational program for patients undergoing lumbar or cervical fusion using VariLift device with the ultimate goal to aid in the development of strategic treatment pathways and improved patient care. All patients who agree to participate in the registry will sign an informed consent form and subsequently be treated by their surgeon with the VariLift device. Potential treatment procedures include bilateral posterior lumbar interbody fusion (PLIF), unilateral transforaminal lumbar interbody fusion (TLIF), or bilateral anterior lumbar interbody fusion (ALIF) for the lumbar spine, or cervical unilateral or bilateral ACDF procedure. Surgical procedures can be performed in either an inpatient or outpatient facility. It is anticipated that the VariLift devices will improve patient outcomes and lead to the development of treatment pathways to improve patient care.