Intra-operative Assessment of the Intellirod LOADPRO Spinal Rod Strain Sensor for Use During Kyphotic Corrective Surgery
NCT02768675 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12
Last updated 2017-08-22
Summary
The LOADPRO Study is an intra-operative, non-significant risk (NSR) case series feasibility assessment of the Intellirod LOADPRO™ System measuring spinal rod strain in long spinal kyphotic corrective constructs.
Conditions
- Kyphosis
- Spinal Fractures
Interventions
- DEVICE
-
LOADPRO
The Intellirod LOADPRO sensor is a single-use, disposable instrument for the intra-operative measurement of posterior instrumented, spine rod strain.
Sponsors & Collaborators
-
Intellirod Spine
lead INDUSTRY
Principal Investigators
-
Richard N Navarro · Intellirod Spine
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-05-31
- Primary Completion
- 2018-06-30
- Completion
- 2018-12-31
Countries
- United States
Study Locations
More Related Trials
-
Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion
NCT06000319 ·Status: ENROLLING_BY_INVITATION
-
A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis
NCT00290862 ·Status: UNKNOWN ·Phase: NA
-
FREE Study - Fracture Reduction Evaluation
NCT00211211 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion
NCT01430299 ·Status: COMPLETED ·Phase: NA
-
Feasibility Study of NL-Prow Interspinous Spacer to Treat Lumbar Spinal Stenosis
NCT01053364 ·Status: UNKNOWN ·Phase: NA
-
INDUCE: A Prospective 2-Year Spine Registry
NCT06971835 ·Status: ENROLLING_BY_INVITATION
-
A Post-marketing Study to Evaluate a Novel Surgical Monitoring Technique Using the EARP Nerve Cuff in TLIF Surgery.
NCT06204900 ·Status: COMPLETED ·Phase: NA
-
Study Using the SpinalStim Device Following Lumbar Fusion Surgery
NCT03176303 ·Status: COMPLETED
-
Robotic-assisted Pedicule Screw Placement
NCT01944553 ·Status: COMPLETED ·Phase: NA
-
Intracept Minimally-invasive PROcedure for VErtebrogenic Back Pain
NCT06827262 ·Status: RECRUITING
-
Scoliosis Surgery Using the PASS® LP System
NCT01019109 ·Status: COMPLETED
-
Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion
NCT01714804 ·Status: COMPLETED ·Phase: NA
-
Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery
NCT00295009 ·Status: COMPLETED ·Phase: NA
-
Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device
NCT06355791 ·Status: RECRUITING ·Phase: NA
-
Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion
NCT02018445 ·Status: COMPLETED ·Phase: NA
-
Assessment of Flow in Cerebrospinal Fluid Shunts With a Wireless Thermal Anisotropy Measurement Device in Asymptomatic Patients
NCT06410885 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Interbody Systems: Post Market Clinical Follow-up Study
NCT04911257 ·Status: TERMINATED
-
Personalized Spine Study Group (PSSG) Registry
NCT04601363 ·Status: RECRUITING
-
Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion
NCT02628210 ·Status: COMPLETED ·Phase: NA
-
Prospective Study To Assess The Safety and Efficacy of the PROW LIF Procedure
NCT01850537 ·Status: UNKNOWN ·Phase: NA
-
Depo-Medrol on Psoas After LLIF
NCT05929755 ·Status: RECRUITING ·Phase: PHASE4
-
Evaluation of Cervical Fusion With DTRAX® Cervical Cage With DTRAX Bone Screw
NCT02694250 ·Status: WITHDRAWN ·Phase: NA
-
Pilot Study to Evaluate Feasibility of DensiProbe Spine Assessing Bone Strength in Spinal Surgery
NCT01126385 ·Status: COMPLETED
-
Neurologic Complications in Spinal Deformity Surgery
NCT01305343 ·Status: COMPLETED
-
The Objective of the Protocol is to Generate Real World Evidence (RWE) Supporting the Safety, Performance, and Health Economics of Using the Regulatory Approved and Commercially Available EARP Interbody System Used During Lumbar Interbody Fusion (LIF) Procedures With the EARP Nerve Cuff Electrode
NCT07020000 ·Status: NOT_YET_RECRUITING