Post Market Clinical Follow-Up Study on the Performance and Safety of Lyoplant®
NCT05441618 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2025-01-13
Summary
Retrospective, single center, single arm PMCF study on the performance and safety of Lyoplant® used for the replacement and extension of connective tissue structures in neurosurgery.
Conditions
- Tumor, Cerebral Ventricle
- Tumor, Cerebellar
- Aneurysm Cerebral
- Trauma, Brain
Interventions
- DEVICE
-
Lyoplant®
replacement and extension of connective tissue structures in neurosurgery
Sponsors & Collaborators
-
Aesculap AG
lead INDUSTRY
Principal Investigators
-
Philipp E Krauss, Dr. · Universitätsklinikum Augsburg AöR
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-04-02
- Primary Completion
- 2024-12-19
- Completion
- 2025-01-10
Countries
- Germany
Study Locations
More Related Trials
-
XLIF® vs. MAS®TLIF for the Treatment of Symptomatic Lumbar Degenerative Spondylolisthesis With or Without Central Stenosis.
NCT01024699 ·Status: COMPLETED
-
Efficacy of a Full-Thickness Placental Allograft in Lumbar Microdiscectomy
NCT03536013 ·Status: TERMINATED ·Phase: NA
-
Study on the Postoperative Complications and Changes in Posterior Cervical Muscle Volume After Cervical Single Open-door Expansive Laminoplasty With Preservation of Muscular Ligament Complex
NCT05001685 ·Status: COMPLETED
-
Evaluate the Safety and Efficacy of Dura Sealant Patch in Reducing CSF Leakage Following Elective Cranial Surgery
NCT04086550 ·Status: COMPLETED ·Phase: NA
-
Assessing Safety of Cervical Spine Fusion With NMP®
NCT07245940 ·Status: NOT_YET_RECRUITING
-
Short-term Clinical Outcome of Cortical Bone Trajectory Compared With the Traditional "Open" and Minimal Invasive Posterior Lumbar Interbody Fusion
NCT05538416 ·Status: RECRUITING
-
A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease
NCT01491425 ·Status: COMPLETED ·Phase: NA
-
Safety Study of Filler Agent Composed of Autologous Mesenchymal Stem Cells and Hyaluronic Acid
NCT02034786 ·Status: UNKNOWN ·Phase: PHASE1
-
Sagittal Plane Correction With Pass-LP Device in Adult Deformity Patients
NCT01635322 ·Status: COMPLETED
-
Postmarket Clinical Follow-Up Study on Arcadius XP L® Interbody Fusion Device
NCT05944081 ·Status: WITHDRAWN
-
Multimodality Neuromonitoring in XLIF
NCT01499680 ·Status: COMPLETED
-
Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease
NCT01491386 ·Status: COMPLETED ·Phase: NA
-
PMCF Study on the Safety and Performance of CESPACE 3D
NCT04477447 ·Status: COMPLETED
-
Safety and Feasibility of Umbilical Cord Wharton's Jelly Allograft Injections for Lumbar Pain
NCT06361485 ·Status: RECRUITING ·Phase: PHASE1
-
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
-
ArcadiusXP L Post Market Clinical Follow-Up
NCT01895426 ·Status: COMPLETED
-
Quintex® Follow-up After One Year Minimum
NCT04489394 ·Status: COMPLETED
-
Radiographic and Clinical Outcomes of PureGen in Posterior Lumbar (PLIF) and Transforaminal Interbody Fusion (TLIF)
NCT01293981 ·Status: TERMINATED
-
Facet Wedge Post Market Study
NCT02203448 ·Status: COMPLETED
-
FIBERGRAFT Aeridyan Posterolateral Fusion Study
NCT07059065 ·Status: RECRUITING ·Phase: NA
-
Advanced Materials Science in XLIF Study
NCT03649490 ·Status: ENROLLING_BY_INVITATION
-
Extreme Lateral Interbody FusionFUSION (XLIF) Versus Posterior Lumbar Interbody Fusion (PLIF)
NCT04589572 ·Status: SUSPENDED ·Phase: NA
-
Pilot Study of rhBMP-2/ACS/LT-CAGE® for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease
NCT01491373 ·Status: COMPLETED ·Phase: NA
-
Safety and Performance of the Elaspine System in the Treatment of the Lumbar Spine
NCT01323543 ·Status: COMPLETED ·Phase: NA
-
Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine
NCT02684045 ·Status: COMPLETED