Clinical trials: Total Hip
Primary Total Hip Arthroplasty
Accuracy of OPS™ Femoral Neck Resection Study
The primary objective of this study is to determine the accuracy of the Optimized Positioning System (OPS™) planning and delivery tools using different types of surgical approaches.
- Trial name
- NCT03956381
- Testing
- Primary Total Hip Replacement with Trinity cup and TriFit TS stem via posterolateral surgical approach., Primary Total Hip Replacement with Trinity cup and MetaFix stem via direct anterior surgical approach
- Where
- United States
- Volunteers
- 55 people
- Sponsor
- Corin
Primary Total Hip Arthroplasty
OPS™ With Direct Anterior Approach (DAA)
A prospective, non-randomized, single-center clinical study to determine the accuracy of a patient-specific instrument (OPS™) for delivering a planned femoral component anteversion and neck resection using a Direct Anterior…
- Trial name
- NCT04319952
- Testing
- Primary Total Hip Replacement with Metafix™ femoral stem and Trinity™ acetabular cup or TriFit-CF™/TriFit-TS™ femoral stem and Trinity™ acetabular cup implanted by a single surgeon.
- Where
- 2 sites in United States
- Volunteers
- 100 people
- Sponsor
- Corin
Total Hip Arthroplasty
Prospective Observational Case Series of Primary Hip Arthroplasty With a Short Cemented Stem (Friendly Short)
Post-marketing observational case series to analyse the functional recover and radiographic outcomes in terms of implant stability and survivorship of primary hip arthroplasty with Friendly short cemented stem.
- Trial name
- NCT04987437
- Testing
- Friendly short stem
- Where
- Italy
- Volunteers
- 100 people
- Sponsor
- Limacorporate S.p.a
Total Knee Arthroplasty; Total Hip Arthroplasty
Health Partner Evaluation at Princeton
This is a prospective, single-center, randomized, comparative, controlled study. Penn Medicine Princeton Medical Center will enroll a total of 296 subjects (18 years or older) who are electing to have total knee or hip…
- Trial name
- NCT03386786
- Testing
- Health Partner, Standard Care
- Where
- United States
- Volunteers
- 127 people
- Sponsor
- DePuy Orthopaedics
Total Knee Arthroplasty; Total Hip Arthroplasty
Health Partner Evaluation at Providence
This is a prospective, mixed methods, multi-center, randomized, comparative, controlled study. Providence Health \& Services will enroll a total of 296 subjects (18 years or older) who are electing to have total knee or hip…
- Trial name
- NCT03443284
- Testing
- Health Partner, Standard Care
- Where
- 3 sites in United States
- Volunteers
- 79 people
- Sponsor
- DePuy Orthopaedics
Primary Total Hip Arthroplasty
Retrospective Observational Cohort Study of SYMBOL CUP DM 1
This is a single-center retrospective observational cohort study of consecutively operated patients who underwent primary total hip arthroplasty with a SYMBOL CUP DM HA hemispherical dual mobility acetabular implant.
- Trial name
- SYMCOR-1 (NCT04209374)
- Testing
- THA with SYMBOL CUP DM HA
- Where
- France
- Volunteers
- 59 people
- Sponsor
- Dedienne Sante S.A.S.
Prosthetic Fixation After Cementless Total Hip Arthroplasty
The Efficacy Study of Aclasta on Prosthetic Fixation in Postmenopausal Women After THA
It's to investigate the efficacy of Zoledronic acid treatment on the early prosthetic fixation in post-menopausal osteoporosis women under cementless total hip arthroplasty after 24-month observation.
- Trial name
- NCT02333344
- Testing
- Zoledronic acid 5mg
- Where
- China
- Sponsor
- Novartis Pharmaceuticals
Aseptic Loosening, Osteolysis
Post-Market Study of the Modular Revision Hip System
The purpose of this study is to examine the short term efficacy of the MRH system as well as determine if operating room time is decreased using this simple, two-tray system.
- Conditions
- Aseptic Loosening, Osteolysis, Traumatic Fracture, Failed Total Hip Implant
- Trial name
- MRHS (NCT01464645)
- Testing
- Modular Revision Hip System
- Where
- 6 sites in United States
- Volunteers
- 16 people
- Sponsor
- Encore Medical, L.P.
Total Hip Replacement
IPC-CALF Versus GEKO in Post-op Total Hip Patients
This study is designed to compare the effect of IPC on post-operative circulation in lower limbs with gekoTM device after total hip replacement procedure.
- Trial name
- NCT02425917
- Testing
- geko, IPC-Calf
- Sponsor
- Firstkind Ltd
Total Hip Resurfacing
Data Collection on ReCap/Magnum in Total Hip Replacement and Resurfacing
Observational study on ReCap/Magnum in Total Hip Replacement and Resurfacing.
- Trial name
- NCT00758355
- Where
- 6 sites in France
- Volunteers
- 150 people
- Sponsor
- Zimmer Biomet
Total Hip Arthroplasty Revision
Post Market Clinical Follow-Up of Acetabular Titan-Augment Structan®
Implant Survival as well as clinical and radiological Follow-Up of acetabular Titan-Augment Structan®
- Trial name
- NCT02019433
- Testing
- Structan®
- Where
- 3 sites in Germany
- Volunteers
- 5 people
- Sponsor
- Aesculap AG
Total Hip Arthroplasty (THA)
REDAPT Revision System Study to Assess 5 Year Revision Rate & up to 10 Year Revision Rate and Safety and Effectiveness
The objective of the study is to demonstrate non-inferiority of stem revision rate in subjects implanted with the REDAPT™ System with a revision rate of less than 9.8% at the 5 year mark assuming an observed rate of 6.5% at 5…
- Trial name
- NCT02344160
- Testing
- Phlebotomy
- Where
- United States
- Sponsor
- Smith & Nephew, Inc.
Pinnacle Metal-on-Metal, Revised Pinnacle Metal-on-Metal
Pinnacle Metal-on-Metal 522 Post-Market Surveillance Study
The purpose of this clinical study is to evaluate blood metal ion levels as a function of time of implantation for the Pinnacle Acetabular MoM system.
- Conditions
- Pinnacle Metal-on-Metal, Revised Pinnacle Metal-on-Metal, Adverse Local Tissue Reaction, Metal Ions
- Trial name
- NCT01828801
- Testing
- Pinnacle Metal-on Metal
- Where
- 8 sites in United States
- Volunteers
- 276 people
- Sponsor
- DePuy Orthopaedics
Adverse Local Tissue Reaction, Total Hip Arthroplasty
ASR-XL Metal-on-Metal 522 Post-Market Surveillance Study
The purpose of this clinical study is to evaluate blood metal ion levels as a function of time of implantation for the ASR-XL MoM system.
- Trial name
- NCT01884532
- Testing
- ASR-XL Metal-on-Metal
- Where
- 7 sites in United States
- Volunteers
- 146 people
- Sponsor
- DePuy Orthopaedics
Primary Total Hip Replacement
A DEXA Clinical Study to Evaluate the Osteointegrative Potential of Trabecular Titanium™
The purpose of this clinical trial is to evaluate the osteointegrative potential of the Trabecular TitaniumTM and to measure the pattern of changing in bone mineral density (BMD) around an uncemented acetabular cup, manufactured…
- Trial name
- NCT02635581
- Testing
- Delta TT acetabular cup
- Where
- 4 sites in Italy
- Volunteers
- 84 people
- Sponsor
- Limacorporate S.p.a
Prophylaxis, Thromboembolism, Venous, Total Knee Replacement
Study to Observe Safety of Xarelto in VTE Prophlylaxis After Elective TKR (Total Knee Replacement) or THR (Total Hip Replacement)
The primary objective of this study is to evaluate the safety of Xarelto in the prophylaxis of VTE in Indian patients undergoing elective TKR/THR
- Conditions
- Prophylaxis, Thromboembolism, Venous, Total Knee Replacement, Total Hip Replacement
- Trial name
- XYRIS (NCT01523418)
- Testing
- Rivaroxaban (Xarelto, BAY59-7939)
- Sponsor
- Bayer
In Need of a Total Hip Arthroplasty
E-MAX 2nd Gen Vit E Poly On BIOLOX Delta Ceramic Heads
The purpose of this study is to monitor outcomes of total hip arthroplasties performed with E-MAX polyethylene and BIOLOX Delta Ceramic head.
- Trial name
- NCT01943149
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Renovis Surgical Technologies, Inc.
Total Hip Replacement System
Ceramic on Metal Total Hip Replacement System Multi-Center,Investigational Device Exemption Clinical Trial
The purpose of this study is to demonstrate non-inferiority of the Ceramic on Metal Total Hip when compared to a TRANSCEND® historical control group of patients with primary total hip replacement.
- Trial name
- COM (NCT00820443)
- Testing
- Ceramic on metal prosthesis
- Where
- United States
- Volunteers
- 253 people
- Sponsor
- MicroPort Orthopedics Inc.
Total Hip Arthroplasty, Muscle Injury
Safety and Efficacy of IM Injections of PLX-PAD for the Regeneration of Injured Gluteal Musculature After Total Hip Arthroplasty
Local administration of PLX-PAD single dose, intra-muscular injection for the regeneration of injured gluteal musculature after Total Hip Arthroplasty (THA).
- Trial name
- NCT01525667
- Testing
- 150M PLX-PAD, 300M PLX-PAD
- Where
- Germany
- Volunteers
- 20 people
- Sponsor
- Pluristem Ltd.
Total Hip Arthroplasty
TRJ Post Market Clinical Follow Up
Clinical and radiological 2 years results of TRJ® Hip Stem.
- Trial name
- NCT02019862
- Testing
- TRJ® Total Hip Arthroplasty
- Where
- Germany
- Volunteers
- 100 people
- Sponsor
- Aesculap AG