Post-Market Study of the ICONACY Hip System
NCT02027974 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2014-05-13
Summary
The purpose of this study is to evaluate the use and efficacy of the Iconacy Hip System for total hip replacement surgery.
Conditions
- Degenerative Joint Disease
Interventions
- DEVICE
-
Iconacy Hip System
Comparison of Iconacy I-Hip system to the Stryker Accolade hip system using a randomized study.
- DEVICE
-
Stryker Accolade Hip System
Comparison of Iconacy I-Hip system to the Stryker Accolade hip system using a randomized study.
Sponsors & Collaborators
-
Iconacy Orthopedic Implants, LLC.
lead INDUSTRY
Principal Investigators
-
William A Hodge, MD · Eastern Maine Medical Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-12-31
- Primary Completion
- 2016-12-31
- Completion
- 2016-12-31
More Related Trials
-
A Prospective, Pre-market, Multi-center Study of Insignia Hip Stem in THA to Determine Implant Survivorship and PROMS.
NCT06108934 ·Status: RECRUITING ·Phase: NA
-
Active Knee Prosthesis Study for Improvement of Locomotion for Above Knee Amputees
NCT00771589 ·Status: UNKNOWN ·Phase: NA
-
Clinical Evaluation of the Integra® Titan™ Modular Shoulder System Generation 2.5 for Primary Shoulder Joint Replacement
NCT03250767 ·Status: TERMINATED
-
A Study to Evaluate the Conformis iTotal Identity Knee Replacement System
NCT04667559 ·Status: TERMINATED
-
Clinical Evaluation of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement (CADENCE)
NCT03142958 ·Status: SUSPENDED
-
Evaluation of the Efficacy of the Bipolar Sealer Aquamantys 6.0 in Patients Undergoing Total Hip Arthroplasty
NCT01027195 ·Status: COMPLETED ·Phase: PHASE4
-
I-beam and Cruciate Tibial Components Used in Total Knee Replacement
NCT00588783 ·Status: TERMINATED
-
Evaluate the Safety and Effectiveness of the Polymotion Hip Resurfacing (PHR) System Compared to Total Hip Arthroplasty
NCT06792539 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Autologous Chondrocyte Implantation in the Patellofemoral Joint
NCT00212849 ·Status: COMPLETED
-
Physica System Total Knee Replacement Registry Study
NCT03048201 ·Status: RECRUITING ·Phase: NA
-
Aequalis Resurfacing Head Study
NCT02444299 ·Status: UNKNOWN
-
LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study
NCT00510458 ·Status: COMPLETED ·Phase: NA
-
A Clinical Investigation of the M2a- 38™ Hip System
NCT00698503 ·Status: TERMINATED
-
Retrospective Encore Reverse Shoulder Prosthesis Study
NCT00765037 ·Status: COMPLETED
-
A Prospective Clinical Study On A Total Hip Resurfacing System
NCT00604734 ·Status: COMPLETED ·Phase: NA
-
Evaluating Cryopreserved Osteochondral Allograft Cores for the Treatment of Osteochondral Lesions in the Knee
NCT06216756 ·Status: RECRUITING ·Phase: NA
-
Total Hip Replacement With the Answer® Hip Stem and Ranawat/Burnstein® Shell Using Simplex® or Palacos® Bone Cement
NCT00588861 ·Status: TERMINATED ·Phase: NA
-
Post-Market Study of the 3DKnee™ System
NCT00819481 ·Status: COMPLETED
-
One-stage Exchange Arthroplasty for Chronic Prosthetic Joint Infections
NCT03473392 ·Status: COMPLETED
-
Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty
NCT03668704 ·Status: ACTIVE_NOT_RECRUITING
-
The 3DKnee™ System: A Post-Market Study
NCT00764673 ·Status: COMPLETED ·Phase: PHASE4
-
Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - Europe
NCT03566082 ·Status: COMPLETED
-
Durom(R) Hip Resurfacing System Multicenter Trial
NCT00746616 ·Status: COMPLETED ·Phase: PHASE3
-
Post Market Clinical Follow-Up of the Zimmer Stafit Acetabular System
NCT04079114 ·Status: TERMINATED
-
Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting
NCT02820766 ·Status: TERMINATED