| Not Yet Recruiting | A Study of the Effect of a Nurse Navigator Program on High Risk Patients NCT05592847 | Mayo Clinic | N/A |
| Not Yet Recruiting | Development and Measurement of the Effects of a Digital Education Solution for Patients Undergoing Total Hip o NCT07345299 | Haute Ecole de Santé Vaud | N/A |
| Completed | Role of Iliotibial Band Stiffness in Perceived Leg Length Discrepancy After Total Hip Arthroplasty NCT07431138 | Ankara Etlik City Hospital | — |
| Recruiting | PENG Block + LIA For Endoprosthesis Surgery With Anterior Approach NCT07239817 | ASST Gaetano Pini-CTO | N/A |
| Active Not Recruiting | Analgesic Efficacy of Continuous S-ESP vs Continuous FICB After Hip Arthroplasty NCT07516795 | Bach Mai Hospital | N/A |
| Not Yet Recruiting | Associations Between Time to Reduction and Complications in Patients With Dislocated Total Hip Arthroplasty NCT07132723 | Nordsjaellands Hospital | — |
| Not Yet Recruiting | Phase IIa Trial of Oral SSS17 for Post-Arthroplasty Anemia NCT07007936 | Shenyang Sunshine Pharmaceutical Co., LTD. | Phase 2 |
| Not Yet Recruiting | Sleep Patterns After Total Joint Replacement Surgery NCT04896892 | Henry Ford Health System | — |
| Completed | Dimolegin® (60 mg) Given Once Daily in Patients Undergoing Total Hip or Knee Replacement Compared to Enoxapari NCT07124819 | Avexima Diol LLC | Phase 3 |
| Unknown | Testing Implementation of Total Joint Replacement Rehabilitation Quality Indicator Toolkits NCT06208553 | University of British Columbia | N/A |
| Recruiting | Low Concentration Local Anesthesia Fascia Iliaca Block for Total Hip Arthroplasty NCT06102811 | University of Toronto | N/A |
| Withdrawn | Study Measuring the Effects of Patient Data for Total Hip and Total Knee Arthroplasty Patients Using an APP Ba NCT05182320 | Aesculap AG | — |
| Completed | Exploring Novel Diagnostic Tools for Periprosthetic Joint Infection NCT05582460 | Rijnstate Hospital | — |
| Unknown | MARS MRI in Revision THA With a Ceramic Femoral Head and Titanium Sleeve NCT05686915 | Colorado Joint Replacement | — |
| Active Not Recruiting | TENS for Relief of Postoperative Pain in Orthopedic Patients NCT05678101 | Karolinska University Hospital | N/A |
| Active Not Recruiting | CGM Monitoring in T2DM Patients Undergoing Orthopaedic Replacement Surgery NCT05666479 | Stony Brook University | — |
| Completed | Effects of Preoperative Education, and Follow-up Sessions of Patients With Total Hip and Knee Arthroplasty (ES NCT05452161 | Haute Ecole de Santé Vaud | N/A |
| Recruiting | Antibiotic Impregnated Bone Graft to Reduce Infection in Hip Replacement. NCT05169229 | University Hospital, Linkoeping | Phase 2 / Phase 3 |
| Completed | Effect of Video Education on Daily Life Quality and Wound Care in Total Hip Arthroplasty Patients NCT06523829 | Bandırma Onyedi Eylül University | N/A |
| Completed | Tranexamic Acid Dosing for Major Joint Replacement Surgery NCT05075200 | Sunnybrook Health Sciences Centre | Phase 2 |
| Completed | Prevention of Bleeding in Total Joint Replacement: Combined Route Administration of Tranexamic Acid NCT05874583 | Mongi Slim Hospital | N/A |
| Unknown | On-Table Versus Off-Table Total Hip Arthroplasty NCT04831372 | Carilion Clinic | N/A |
| Completed | Does Rehabilitation After Total Hip Or Knee Arthroplasty Work (DRAW2) NCT04960241 | Troels Mark Christensen | N/A |
| Completed | RCT Measuring the Effect of the ERVIN Software NCT04332055 | Northern Orthopaedic Division, Denmark | N/A |
| Completed | Reducing Postoperative Side Effect of Pregabalin NCT04599894 | The First Hospital of Jilin University | Phase 4 |
| Completed | PMCF 8 Year Results TRJ® NCT04542174 | Aesculap AG | — |
| Completed | Promotion and Support for Physical Activity Maintenance Post Total Hip Arthroplasty NCT04471532 | Bispebjerg Hospital | N/A |
| Completed | Combined PENG and LFCN Block for Total Hip Arthroplasty NCT04996290 | University Hospital, Antwerp | N/A |
| Active Not Recruiting | A Post Market Clinical Follow-up Study With the aneXys Cup NCT03274830 | Mathys Ltd Bettlach | — |
| Unknown | Effect of Cuff Pressure During Operation on Postoperative Sore Throat NCT04247360 | Keimyung University Dongsan Medical Center | N/A |
| Withdrawn | Does Testosterone Therapy Improve Patient-Reported Outcomes in Age-Related Testosterone Deficient Patients Und NCT05722301 | American Hip Institute | Phase 3 |
| Unknown | Comparing Short-term Outcomes After Direct Anterior and SuperPATH Hip Arthroplasty Approaches NCT03746925 | Ottawa Hospital Research Institute | N/A |
| Unknown | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis NCT04019925 | Unity Health Toronto | N/A |
| Unknown | Pillow Use During Total Hip Arthroplasty NCT03825029 | Ottawa Hospital Research Institute | N/A |
| Terminated | Goal Directed Fluid Therapy Versus Liberal Fluid Regimen in Primary Elective Hip Artrhoplasty NCT04996420 | Istituto Ortopedico Rizzoli | N/A |
| Unknown | Impact of Integrated Care Pathways for Prevention of Post-operative Urinary Retention (POUR) NCT03863743 | TriHealth Inc. | N/A |
| Completed | Does Rehabilitation After Total Hip and Knee Arthroplasty Work NCT03750448 | Bornholms Regionskommune | N/A |
| Completed | Functional Outcomes and Quality of Life in Hip, Knee and Shoulder Arthroplasty NCT03790267 | Istituto Ortopedico Rizzoli | — |
| Unknown | Gait Analysis and Gait Training in Patient With Total Hip or Total Knee Replacement NCT03849638 | Campus Bio-Medico University | N/A |
| Unknown | Postoperative Outcomes Within an Enhanced Recovery After Surgery Protocol (POWER2) NCT03570944 | Grupo Español de Rehabilitación Multimodal | — |
| Completed | Pelvic Inclination Measurement by Navigated Ultrasound NCT03555812 | University Hospital, Brest | N/A |
| Completed | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH NCT03499028 | The Cleveland Clinic | N/A |
| Completed | Improvement of Patient Satisfaction and Overall Outcomes Using HealthLoop NCT03481595 | The Cleveland Clinic | N/A |
| Completed | Home-based Rehabilitation Following a Total Hip Replacement NCT03109821 | Central Jutland Regional Hospital | — |
| Withdrawn | Longjohn Amgen Study - Effect of Denosumab... NCT02444585 | University of Southern California | Phase 1 |
| Active Not Recruiting | Trident II Tritanium Acetabular Shell Outcomes Study NCT02999009 | Stryker Orthopaedics | N/A |
| Completed | The Effectiveness of Rehabilitation in Gait Recovery After Knee or Hip Arthroplasty NCT04803578 | Fondazione Don Carlo Gnocchi Onlus | — |
| Unknown | Intravenous vs. Topical Tranexamic Acid in Revision THA (VITALITY-X) NCT02938962 | Mount Sinai Hospital, Canada | Phase 4 |
| Completed | A Study of Patients Undergoing Total Knee and Hip Arthroplasty at a Regional Hospital in Denmark NCT03008967 | Bornholms Regionskommune | — |
| Completed | Effects of Photobiomodulation Therapy (PBMT) in Total Hip Arthroplasty NCT02970890 | Adriane Aver Vanin | N/A |
| Unknown | Benchmarking the iOS Balance Application Against the Berg Balance Test NCT02705690 | Stannah Stairlifts | N/A |
| Completed | Antibiotic Prophylaxis in Primary Joint Arthroplasty of the Hip and Knee. NCT03348254 | Onze Lieve Vrouwe Gasthuis | — |
| Completed | Effects of Surgery Start Time on Postoperative Interleukin-6, Interleukin-8, and Cortisol NCT03076827 | Chuncheon Sacred Heart Hospital | N/A |
| Completed | Does Rapid Mobilisation Improve Length of Stay and Outcomes Post THR NCT02428829 | The Royal Bournemouth Hospital | N/A |
| Withdrawn | iCORE: Collaborative Orthopedics Outcomes Registry NCT02422667 | SCRI Development Innovations, LLC | — |
| Completed | Patent Foramen Ovale and the Risk of Postoperative Delirium Following Elective Hip and Knee Arthroplasty Surge NCT02400892 | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's | — |
| Completed | Effect of Nervus Cutaneous Femoris Lateralis-Blockade on Moderate Pain Responders After Total Hip Arthroplasty NCT02344264 | Daniel Hägi-Pedersen | Phase 4 |
| Unknown | An Intravenous Iron Based Protocol for Preoperative Anaemia in Hip and Knee Surgery - An Observational Study NCT02385383 | Rigshospitalet, Denmark | — |
| Completed | The Effect of Spouses' Involvement Through Case Management in Older Patients' Fast-track Program NCT02561637 | University of Aarhus | N/A |
| Completed | Functional Movement Retraining After Hip Replacement NCT01878175 | VA Office of Research and Development | N/A |
| Completed | Ultrasound Guided Fascia Iliaca Block for Pain Control After Elective Hip Replacement Surgery NCT02108847 | University of Saskatchewan | N/A |
| Completed | Effect of a Lateral Nerve of the Thigh Block on Postoperative Pain After Total Hip Replacement Surgery NCT02289937 | Daniel Hägi-Pedersen | Phase 4 |
| Terminated | Secur-Fit Advanced Outcomes Study NCT01917929 | Stryker Orthopaedics | N/A |
| Completed | Lower Limb Blood Flow Geko vs Foot Pump NCT03317145 | Hampshire Hospitals NHS Foundation Trust | N/A |
| Unknown | Incidence and Reasons for Preoperative Anemia in Elective Lower Joint Arthroplasty NCT02385409 | Oeivind Jans | — |
| Active Not Recruiting | Multicentre Prospective Study to Evaluate Long-term Clinical Outcomes of the Sirius Cemented Femoral Stem NCT02371382 | Zimmer Biomet | — |
| Unknown | The Effect of Isokinetic Strengthening Training NCT02938416 | Taichung Veterans General Hospital | N/A |
| Completed | Oxycodone Versus Intravenous Morphine for Postoperative Analgesia After Hip Surgery NCT01536301 | Centre Hospitalier Universitaire de Nīmes | Phase 4 |
| Completed | ATX Register Accolade Stem & Trident/Tritanium Cup With X3 Insert NCT02520544 | Stryker Orthopaedics | N/A |
| Completed | Reversal of Neuromuscular Blockade With Sugammadex or Usual Care in Hip Fracture Surgery or Joint (Hip/Knee) R NCT01422304 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | Russian Non-Interventional Study on Compliance of Venous Thromboembolism (VTE) NCT01444586 | Bayer | — |
| Terminated | Tritanium® Primary Acetabular Shell Study NCT01063751 | Stryker Orthopaedics | N/A |
| Terminated | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study NCT01420237 | Stryker Orthopaedics | N/A |
| Terminated | Pelvic Alignment Level (PAL) Instrument Evaluation NCT01312428 | Stryker Orthopaedics | N/A |
| Completed | Rejuvenate Modular Outcomes Study NCT01257568 | Stryker Orthopaedics | N/A |
| Terminated | A Comparative Study of In-vivo Wear Between 28 mm and 40 mm Metal Heads NCT02525627 | Stryker Orthopaedics | N/A |
| Unknown | Evaluation of Four Surgical Techniques in Primary Total Hip Arthroplasty NCT01031732 | Chang Gung Memorial Hospital | N/A |
| Unknown | Retrospective Chart Analysis in the Effective Use of FloSeal in Post-Operative Joint Replacements NCT00958945 | Desert Orthopedic Center Medical Research Foundation | — |
| Completed | Use of Local Analgesia With Epinephrine During Total Hip Arthroplasty (THA) NCT00980616 | University Hospital, Clermont-Ferrand | Phase 2 |
| Unknown | Cementless New Alumina-zirconia Ceramic Bearing Total Hip Arthroplasty (THA) in Asian Patients NCT00935519 | Seoul National University Bundang Hospital | N/A |
| Completed | Comparison in Need for Bank Blood Between Patients Undergoing Total Hip Surgery That Either Receive Their Own NCT00822588 | Wellspect HealthCare | N/A |
| Completed | A Study Evaluating Efficacy and Safety of YM150 Compared to Enoxaparin in Subjects Undergoing Hip Replacement NCT00902928 | Astellas Pharma Europe B.V. | Phase 2 / Phase 3 |
| Terminated | Study to Evaluate the Safety and Efficacy of Pradaxar for the Prevention of Venous Thromboembolism in the Mexi NCT00967447 | Boehringer Ingelheim | — |
| Completed | Ketamine Associated With Morphine PCA After Total Hip Arthroplasty NCT00797264 | Assistance Publique - Hôpitaux de Paris | N/A |
| Completed | Walking Skill Training Program Effects in Patients With Total Hip Arthroplasty NCT00808483 | University of Oslo | N/A |
| Completed | Visibility of Site Marking for Surgical Time Out With Two Different Skin Preparation Solutions NCT00739583 | Johns Hopkins University | Phase 4 |
| Completed | A Phase 2b Study of DU-176b, Prevention of Venous Thromboembolism in Patients After Total Hip Arthroplasty NCT01203098 | Daiichi Sankyo Co., Ltd. | Phase 2 |
| Completed | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study NCT00510458 | Stryker Orthopaedics | N/A |
| Completed | Trident® Tritanium™ Acetabular Shell Revision Study NCT00535626 | Stryker Orthopaedics | N/A |
| Completed | Benefits of 'Repeat Back' Protocols Within A Computer-Based Informed Consent Program NCT00288899 | VA Office of Research and Development | Phase 1 |
| Completed | Total Hip Replacement Study With XRP4563 (Enoxaparin Sodium) NCT00349180 | Sanofi | Phase 3 |
| Completed | Tranexamic Acid vs. Quixil - Reducing Blood Loss in Joint Replacement NCT00378872 | Golden Jubilee National Hospital | N/A |
| Completed | The Comparison of 32mm and 28mm Head Components in Alumina-alumina Total Hip Arthroplasty NCT01098604 | Seoul National University Bundang Hospital | Phase 4 |
| Completed | Accolade® TMZF® Hip Stem Outcomes Study NCT00957658 | Stryker Orthopaedics | N/A |
| Unknown | The Effectiveness of Two Osteoporosis Drugs on Prosthetic Bone Mineral Density (BMD) Loss After Total Hip Arth NCT01020253 | Yokohama City University Medical Center | N/A |
| Completed | Trident® X3 Polyethylene Insert Study NCT00958191 | Stryker Orthopaedics | N/A |
| Completed | Alberta Hip and Knee Replacement Project NCT00277186 | Alberta Bone and Joint Health Institute | N/A |
| Completed | Intraarticular Analgesia After Total Hip Arthroplasty, a Randomised Study NCT00289419 | University of Aarhus | Phase 4 |
| Withdrawn | Tranexamic Acid Study NCT00375440 | Texas Tech University Health Sciences Center | N/A |
| Completed | Study of the Efficacy and Safety of DU-176b in Preventing Blood Clots in Patients Undergoing Total Hip Replace NCT00107900 | Daiichi Sankyo | Phase 2 |
| Completed | Dabigatran Etexilate in Extended Venous Thromboembolism (VTE) Prevention After Hip Replacement Surgery NCT00168818 | Boehringer Ingelheim | Phase 3 |
| Completed | Alberta Hip Improvement Project NCT00293774 | Alberta Bone and Joint Health Institute | — |
| Completed | Restoration® Modular Revision Hip System Post Market Study NCT00962013 | Stryker Orthopaedics | N/A |
| Completed | Posterolateral Surgical Approach Compared With Modified Lateral Approach NCT00936949 | Seoul National University Bundang Hospital | N/A |
| Completed | Expectations, Satisfaction and Quality of Life in Total Hip Arthroplasty NCT00197990 | Hospital for Special Surgery, New York | — |
| Completed | ABC/Trident® Ceramic Post Approval Study NCT00960206 | Stryker Orthopaedics | N/A |
| Completed | Prevention of Ectopic Bone Related Pain and Disability After Hip Replacement Surgery With Peri-Operative Ibupr NCT00145730 | The George Institute | Phase 4 |
| Completed | Addressing Patients' Expectations of Total Hip Arthroplasty in a Randomized Trial NCT00198003 | Hospital for Special Surgery, New York | N/A |
| Terminated | Omnifit Hydroxylapatite (HA) Hip Outcomes Study NCT00958347 | Stryker Orthopaedics | N/A |