PMCF Study on the Safety & Performance of CESPACE 3D

See also
Status	Clinical Trial	Phase
Recruiting	`NCT03883022` - Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery	N/A
Active, not recruiting	`NCT04542577` - PMCF Study on the Safety and Performance of PROSPACE 3D / PROSPACE 3D OBLIQUE / TSPACE 3D
Completed	`NCT02558621` - New Robotic Assistance System for Spinal Fusion Surgery	N/A
Terminated	`NCT01461005` - A Postmarket Surveillance Study of the Paradigm Spine Dynamic Stabilization System (DSS)	N/A
Completed	`NCT00405691` - Safety and Effectiveness Study of the TOPS System, a Total Posterior Arthroplasty Implant Designed to Alleviate Pain Resulting From Moderate to Severe Lumbar Stenosis	Phase 3
Completed	`NCT00205101` - Clinical Outcome Study of the Triad Allograft for Posterior Lumbar Fusion
Enrolling by invitation	`NCT04204135` - The Course of Hip Flexion Weakness Following LLIF or ALIF
Recruiting	`NCT05238740` - Comparison of Standalone Anterior Lumbar Interbody Fusion (ALIF) L5/S1 Performed With Either rhBMP-2 or ViviGen®	N/A
Not yet recruiting	`NCT02805985` - Post-market Surveillance Study of FLXfit™ TLIF Interbody Fusion Device	N/A
Completed	`NCT02966639` - Validation of Appropriateness Criteria for the Surgical Treatment of Lumbar Degenerative Spondylolisthesis
Completed	`NCT02931279` - PASS OCT® Post-market Clinical Follow-up
Active, not recruiting	`NCT02057744` - MIS ReFRESH: Robotic vs. Freehand Minimally Invasive Spinal Surgeries
Completed	`NCT01711203` - The Addition of a Pilates Program for Short-Term Improvements in Patients With Spondylolysis or Spondylolisthesis	N/A
Completed	`NCT00549913` - Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF)	Phase 1/Phase 2
Terminated	`NCT00254852` - Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft	N/A
Terminated	`NCT00095095` - Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™ Fusion Device	Phase 4
Active, not recruiting	`NCT03956537` - PMCF Neo Pedicle Screw and Cage Systems
Recruiting	`NCT05182489` - Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages	N/A
Completed	`NCT02884440` - Transverse Abdominis Plane Block for Anterior Approach Spine Surgery	Phase 2
Enrolling by invitation	`NCT02958241` - Supine vs. Upright Weight Bearing MRI in the Evaluation of Patients With Lumbar Spondylolisthesis	N/A

NCT number	NCT04477447
Study type	Observational
Source	Aesculap AG
Contact	Stefan Maenz, Dr.
Phone	+49-7461-95-0
Email	stefan.maenz@aesculap.de
Status	Recruiting
Phase
Start date	September 21, 2020
Completion date	June 2024

PMCF Study on the Safety and Performance of CESPACE 3D — CATALINA

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms