Evolusion Study Using the Zyga SImmetry Sacroiliac Joint Fusion System
NCT02074761 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 250
Last updated 2020-10-12
Summary
Sacroiliac joint pain reduction and radiographic evidence of SIJ fusion will be collected to evaluate clinical performance of the SImmetry Sacroiliac Joint Fusion System.
Conditions
- Sacroiliac Joint Dysfunction
Interventions
- DEVICE
-
SImmetry
The SImmetry device is commercially available. The implanted devices consist of a range of threaded, self-tapping, cannulated implants designed to transfix the sacrum and ilium, providing stability for intra-articular fusion. The SImmetry Surgical Instruments include standard manual surgical instruments used to access and prepare the sacroiliac joint space for intra-articular fusion.
Sponsors & Collaborators
-
Surgalign Spine Technologies
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-06
- Primary Completion
- 2019-08-31
- Completion
- 2020-11-30
Countries
- United States
Study Locations
More Related Trials
-
Sacroiliac Joint Fusion With iFuse Implant System (SIFI)
NCT01640353 ·Status: COMPLETED
-
Sacroiliac Joint Fusion Comparison Study
NCT03230279 ·Status: WITHDRAWN ·Phase: NA
-
Safety And Efficacy Assessment of the zLock Facet Fusion System- A Pilot Study
NCT04229316 ·Status: COMPLETED ·Phase: NA
-
Investigation of Sacroiliac Fusion Treatment (INSITE)
NCT01681004 ·Status: COMPLETED ·Phase: NA
-
Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices
NCT07204288 ·Status: RECRUITING ·Phase: NA
-
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
NCT00726310 ·Status: COMPLETED
-
Sacroiliac (SI) Joint Transfixing and Fusion: Meaningful Long Term Outcomes With Nevro1
NCT06909292 ·Status: RECRUITING
-
Fluoroscopically-guided Versus Landmark-guided Sacroiliac Joint Injections
NCT02096653 ·Status: COMPLETED ·Phase: NA
-
Prospective Clinical Evaluation of the New Aegis Plate for Anterior Interbody Fusions
NCT00555659 ·Status: COMPLETED
-
Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion
NCT06487936 ·Status: RECRUITING
-
Spineology Clinical Outcomes Trial: An IDE Investigation
NCT02347410 ·Status: COMPLETED ·Phase: NA
-
Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOK
NCT01861899 ·Status: COMPLETED
-
Adjacent Level Anterior Cervical Fusion: SeaSpine Shoreline Versus Removal of Previously Implanted Plate and Replating
NCT06415136 ·Status: ENROLLING_BY_INVITATION
-
Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device
NCT06355791 ·Status: RECRUITING ·Phase: NA
-
iFuse TORQ for the Treatment of Sacroiliac Joint Dysfunction
NCT05870488 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System
NCT00758719 ·Status: COMPLETED
-
Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery
NCT00295009 ·Status: COMPLETED ·Phase: NA
-
Retrospective/Prospective Data Collection on the LDR ROIA Interbody Fusion Device With VerteBRIDGE Plating
NCT02104141 ·Status: COMPLETED
-
Safety and Efficacy Assessment of Using the zLOCK Facet Stabilization System
NCT05266521 ·Status: RECRUITING ·Phase: NA
-
Prospective SPINE Registry
NCT04176562 ·Status: RECRUITING
-
Real World Data Collection on the Synergy Disc
NCT06383949 ·Status: RECRUITING
-
SynerFuse Spinal Fusion and Neuromodulation Proof of Concept Study
NCT04054401 ·Status: RECRUITING ·Phase: NA
-
Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion
NCT01430299 ·Status: COMPLETED ·Phase: NA
-
Use of Radiostereometric Analysis (RSA) Following Spinal Fusion Versus the DYNESYS Stabilization System
NCT00152165 ·Status: COMPLETED
-
Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion
NCT01714804 ·Status: COMPLETED ·Phase: NA