RAMP Study: A Study Comparing Two Lumbar Fusion Procedures

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

TERMINATED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-06-30

Study Completion Date

2014-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a post-marketing, on-label Efficacy, Effectiveness and Safety Study designed in a Multicenter, Randomized, Prospective format. This study compares two spinal fusion procedures, Transacral Interbody Fusion and Transforaminal Lumbar Interbody Fusion (TLIF). Enrollment period will be approximately 12-18 months; each Principal Investigator/Study Center will be expected to enroll up to 20 subjects. The protocol requires approximately 7 subject visits to the study center from screening through the final follow-up visit.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

A Study Comparing Fusion Rates of Two Lumbar Fusion Procedures

NCT01972256

Pseudoarthrosis Spinal Stenosis Spondylolisthesis +1 more

COMPLETED

Comparison of Posterior Cellular Bonegraft Options for Single Level Lumbar Spinal Fusion

NCT07187362

Disc Degenerative Disease Spine Fusion for Degenerative Spine Disease

COMPLETED PHASE2/PHASE3

Retrospective, Multicenter Clinical Evaluation of Health Economic Drivers and Complications for Two Lumbar Fusion Procedures

NCT02171169

Spinal Stenosis Spondylolisthesis Degenerative Disc Disease (DDD)

UNKNOWN

Pilot Study of rhBMP-2/ACS/LT-CAGE® for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease

NCT01491373

Degeneration of Lumbar Intervertebral Disc

COMPLETED NA

Interbody Systems: Post Market Clinical Follow-up Study

NCT04911257

Degenerative Disc Disease

TERMINATED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Study Treatment Arms:

The transacral lumbar interbody fusion (including 1L+ and 2L+) is a minimally invasive technique that uses a transacral approach to achieve fusion at the L5-S1 or L4-L5-S1 spinal levels. The transforaminal lumbar interbody fusion (TLIF) is performed by using a posterior unilateral or bilateral incision in which the lumbar spine is accessed. Both study procedures are approved for use and conform to US regulatory requirements. The study employs these procedures and devices for uses that are consistent with their 510(k), legally cleared, labeling.

Study Design, Objective:

The study objective is to demonstrate non-inferiority between the transacral lumbar interbody fusion procedure and the transforaminal lumbar interbody fusion procedure (TLIF) by meeting the primary and secondary study endpoints as listed below.

Study design, Endpoints:

Primary Endpoint:

Efficacy: Fusion of the targeted vertebral bodies (L4-L5 or L5-S1) by 24 months as determined by Central Radiographic Reviewer's interpretation of high resolution Computed Tomography (CT) scan.

Secondary Endpoints:

Safety: Incidence of major device-related adverse events and/or failures by 24 months, defined as those requiring revision surgery or a secondary operation, or events resulting in permanent disability or death.

Clinical Effectiveness: A 20% decrease in back pain compared to baseline by 24 months as measured by the Visual Analog Scale (VAS) score.

Clinical Effectiveness: A 20% decrease in disability compared to baseline by 24 months as measured by the Oswestry Disability Index (ODI).

Study Design, Enrollment and Analyses:

Approximately 200 subjects will be enrolled in this study and will receive one of two study treatments in the study. The enrollment period is expected to last approximately 18 months, with a 24 month follow up period. Approximately 15-20 sites will participate, and Investigators must be proficient in both of the lumbar fusion procedures.

Analyses:

Eight evaluations: Pre-Operative, Operative, Discharge, and at 1, 3, 6, 12, and 24 Months.

Safety and efficacy analyses will be performed at all follow-up points during the study as well as a final analysis when all subjects have completed the study.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Spinal Stenosis Spondylolisthesis Degenerative Disc Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

transacral lumbar interbody fusion procedure

No interventions assigned to this group

transforaminal lumbar interbody fusion procedure (TLIF)

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Male or female subject that is eligible for both study procedures only at the L4-L5-S1 or L5-S1 levels with bilateral pedicle screws;
* The subject has a diagnosis of one or more of the following conditions at the L4-L5-S1 or L5-S1 levels:

* Spinal stenosis;
* Spondylolisthesis;
* Degenerative Disc Disease (DDD) defined as back pain and/or radicular pain with degeneration of the disc as confirmed by history, physical examination and radiographic studies, either by CT, MRI, plain film, myelography, or discography;
* Adult 18 years of age or older;
* The subject has undergone at least 6 consecutive months of Conservative Care Therapy(ies);
* The subject is able and willing to give written informed consent and to comply with the requirements of this study protocol.

Exclusion Criteria

* Coagulopathy;
* Bowel disease (e.g. Crohn's, ulcerative colitis);
* Severe scoliosis (curves \> 60°);
* Sacral agenesis;
* Spondylolisthesis greater than Grade 1 at the L4-L5-S1 levels, or greater than Grade 2 at the L5-S1 level;
* Spinal tumor (or history of sacral tumor);
* History of fracture at L4, L5 and/or S1 vertebral bodies;
* The subject has undergone a prior fusion procedure of the lumbar spine;
* Osteoporosis; or, if the subject is at high risk for development of osteoporosis, further screening to be conducted at Investigator's discretion;
* Per the Investigator, body weight is exclusionary only if concomitant medical issues are present that preclude the subject from being a candidate for spinal surgery; The subject is a current cigarette smoker;
* For women of childbearing potential, pregnancy at the time of enrollment, or planning to become pregnant during the course of the study;
* The subject has a history of substance abuse (illegal drugs, prescription drugs, or alcohol) that, in the Investigator's opinion, may interfere with protocol assessments and/or the subject's ability to comply with the protocol;
* Per the Investigator, the subject is in poor general health or undergoing any concurrent disease process that would place the subject in excessive risk to surgery (e.g. significant circulatory problems, cardiac disease, history of bowel surgery);
* The subject is participating in another spine study, which, in the opinion of the Investigator, could skew results;
* The subject is involved in litigation related to their back condition;
* The subject is contraindicated to receive either study procedure;
* The subject is contraindicated to receive bilateral pedicle screws;
* The subject has a history of allergy to any component of the devices or biologic material to be implanted in either procedure;
* The subject is a prisoner, transient, or an illegal alien.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No