OsteoFlo HydroFiber Ambispective Evaluation
NCT07784673 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2026-08-27
Summary
The goal of this observational, ambispective study is to collect real world patient outcomes to characterize the safety and effectiveness of OsteoFlo HydroFiber when used to promote fusion in the lumbar spine.
Conditions
- OsteoFlo HydroFiber
Interventions
- DEVICE
-
OsteoFlo HydroFiber
Observational study of subjects previously implanted with OsteoFlo HydroFiber.
Sponsors & Collaborators
-
SurGenTec LLC
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-09-01
- Primary Completion
- 2027-02-01
- Completion
- 2027-02-01
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft
NCT00254852 ·Status: TERMINATED ·Phase: NA
-
Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion
NCT01714804 ·Status: COMPLETED ·Phase: NA
-
Osteocel® Plus in Transforaminal Lumbar Interbody Fusion (TLIF)
NCT00947583 ·Status: COMPLETED
-
Osteocel® Plus in Anterior Lumbar Interbody Fusion (ALIF)
NCT00948831 ·Status: COMPLETED
-
FIBERGRAFT Aeridyan Posterolateral Fusion Study
NCT07059065 ·Status: RECRUITING ·Phase: NA
-
Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion
NCT01018771 ·Status: COMPLETED ·Phase: NA
-
A Prospective Analysis of the Efficacy of Allosync Expand and Autograft Bone Graft in Open Lumbar Spinal Fusion
NCT06415110 ·Status: ENROLLING_BY_INVITATION
-
Evidence For Fusion In Spine With Orthoss®
NCT03853356 ·Status: ACTIVE_NOT_RECRUITING
-
Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices
NCT07204288 ·Status: RECRUITING ·Phase: NA
-
Ultrasound as Adjunct Therapy for Increasing Fusion Success After Lumbar Surgery
NCT00744861 ·Status: TERMINATED ·Phase: NA
-
Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic Infinity Occipitocervical-Upper Thoracic (OCT) System
NCT04056520 ·Status: COMPLETED
-
Evaluation of NB1 Bone Graft Following Lumbar Interbody Arthrodesis
NCT03810573 ·Status: RECRUITING ·Phase: NA
-
Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease
NCT02070484 ·Status: TERMINATED ·Phase: NA
-
Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion
NCT04679844 ·Status: RECRUITING ·Phase: NA
-
Artoss Prospective Spine Registry Outcomes
NCT04439032 ·Status: ACTIVE_NOT_RECRUITING
-
Sterile Amniotic Fluid Filtrate Epidural Injection.
NCT04537026 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion
NCT01873586 ·Status: COMPLETED ·Phase: NA
-
Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion
NCT01013389 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of GENEX® DS in Instrumented Posterolateral Fusion
NCT02317185 ·Status: TERMINATED
-
Lumbar Fusion With Nanotube Versus Titanium Cage
NCT07777718 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
NanOss Bioactive With Autograft and Bone Marrow Aspirate in the Posterolateral Spine
NCT02005341 ·Status: WITHDRAWN ·Phase: NA
-
The OsteoStrand Plus Deformity Study
NCT04629794 ·Status: UNKNOWN ·Phase: NA
-
OssDsign® Spine Registry Study ("Propel")
NCT05329129 ·Status: RECRUITING
-
Comparison of Actifuse ABX and Local Bone in Spinal Surgery
NCT01852747 ·Status: TERMINATED ·Phase: PHASE4
-
Interbody Systems: Post Market Clinical Follow-up Study
NCT04911257 ·Status: TERMINATED