MDR - Longevity IT Oblique and Offset Liners
NCT05980234 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6
Last updated 2024-12-27
Summary
The objective of this retrospective enrollment/prospective follow-up consecutive series PMCF study is to collect data confirming safety, performance, and clinical benefits of the Longevity IT Oblique and Offset liners when used for primary or revision total hip arthroplasty (implants and instrumentation) at a minimum of 10-year follow-up.
Conditions
- Non-inflammatory Degenerative Joint Disease (NIDJD)
- Avascular Necrosis
- Protrusio Acetabuli
- Traumatic Arthritis
- Slipped Capital Femoral Epiphyses
- Fracture of the Pelvis
- Diastrophic Variant
- Osteoarthritis
- Fused Hip
Interventions
- DEVICE
-
Total Hip Arthroplasty with Longevity IT Oblique Liners
Primary or Revision Total Hip Arthroplasty using the Longevity IT Oblique liners according to the approved indications and compatible device.
- DEVICE
-
Total Hip Arthroplasty with Longevity IT Offset Liners
Primary or Revision Total Hip Arthroplasty using the Longevity IT Offset liners according to the approved indications and compatible device.
Sponsors & Collaborators
-
Zimmer Biomet
lead INDUSTRY
Principal Investigators
-
Hillary Overholser · Zimmer Biomet
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-08-30
- Primary Completion
- 2024-11-02
- Completion
- 2024-11-07
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Vivacit-E Post-market Follow-up Study
NCT03226808 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
MDR - PMCF Study for RingLoc Bipolar Acetabular Cup and Endo II Femoral Heads
NCT05199870 ·Status: ENROLLING_BY_INVITATION
-
SCP® Observational Study of the Knee
NCT03110224 ·Status: TERMINATED
-
A Prospective, Randomized, Controlled Study Comparing Three Tibial Component Designs in Total Knee Arthoplasty
NCT00589147 ·Status: COMPLETED ·Phase: NA
-
LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study
NCT00510458 ·Status: COMPLETED ·Phase: NA
-
SCP Hip Outcomes Study
NCT03494660 ·Status: COMPLETED
-
Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient Population
NCT02087449 ·Status: TERMINATED
-
Zimmer Biomet Shoulder Arthroplasty PMCF Study
NCT06920459 ·Status: RECRUITING
-
MDR - Comprehensive Primary Revision Stems PMCF
NCT06788717 ·Status: RECRUITING
-
Clinical Performance of XPEO-E Liner in SERF Dual-mobility Cups
NCT06917365 ·Status: RECRUITING
-
Bone Mineral Density Changes Under Two Tibial Components in Total Knee Arthroplasty
NCT01764984 ·Status: COMPLETED ·Phase: PHASE4
-
MDR - Comprehensive Primary/Micro Stem & Versa-Dial Ti Humeral Head
NCT04003311 ·Status: ENROLLING_BY_INVITATION
-
Long-Term Multi-center Evaluation of E-Poly and Regenerex
NCT00545285 ·Status: UNKNOWN ·Phase: NA
-
Rejuvenate Modular Outcomes Study
NCT01257568 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow Lesions
NCT01621893 ·Status: COMPLETED
-
A Clinical Investigation of the M2a- 38™ Hip System
NCT00698503 ·Status: TERMINATED
-
Total Hip Replacement With the Answer® Hip Stem and Ranawat/Burnstein® Shell Using Simplex® or Palacos® Bone Cement
NCT00588861 ·Status: TERMINATED ·Phase: NA
-
Autologous Osteoblastic Cells Implantation to Early Stage Osteonecrosis of the Femoral Head
NCT02890537 ·Status: COMPLETED ·Phase: PHASE2
-
Clinical and Radiographic Outcomes of the JointMedica Polymotion Resurfacing (PHR) Device
NCT07080671 ·Status: NOT_YET_RECRUITING
-
Use of BMAC With Hip Arthroscopy Treatment of FAI and Labral Tear
NCT03909139 ·Status: RECRUITING
-
Comparison of A Mobile-Bearing Total Knee System With A Fixed-Bearing Total Knee System In Cemented Total Knee Arthroplasty
NCT00589108 ·Status: COMPLETED ·Phase: NA
-
PINNACLE® DM RSA Study
NCT05357664 ·Status: TERMINATED ·Phase: NA
-
Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement
NCT03247023 ·Status: TERMINATED
-
Maxera Large Cups - Canada
NCT04348968 ·Status: TERMINATED
-
Continuation of Patient Follow-up to 2 Years for the Pinnacle RSA and Pinnacle DM RSA Clinical Trials
NCT05930067 ·Status: COMPLETED ·Phase: NA