Clinical trials: Total Knee Replacement Surgeries
Osteoarthritis, Contracture
Reducing Recurrent Knee Flexion Contracture by Correcting Leg Length Discrepancy After Total Knee Arthroplasty for OA
Moving one's joints through their full range of motion (ROM) is crucial for health and wellbeing. Those who are unable to do so have difficulty carrying out simple activities like walking or feeding themselves.
- Trial name
- NCT02861521
- Testing
- Shoe lift
- Where
- Canada
- Volunteers
- 4 people
- Sponsor
- Ottawa Hospital Research Institute
Knee Replacement, Knee Replacement Surgery
Effect of Virtual Reality on Patient Outcomes and Satisfaction in Total Knee Replacement
This study aims to evaluate the effectiveness of virtual reality (VR) in managing preoperative anxiety and postoperative pain in patients undergoing total knee replacement.
- Conditions
- Knee Replacement, Knee Replacement Surgery, Postoperative Pain, Acute, Anxiety, Preoperative
- Trial name
- NCT06933732
- Testing
- Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (2 hours), Device: Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (4 hours), Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (6 hours)
- Where
- Turkey (Türkiye)
- Volunteers
- 64 people
- Sponsor
- Aykut Turgut
Total Hip and Knee Arthroplasties
Teicoplanin Prophylaxis for Total Hip or Knee Arthroplasty
This is a prospective, open-label, randomized clinical trial where patients were administered prophylaxis for total hip or knee arthroplasty either with teicoplanin or with other antibiotics.
- Trial name
- NCT00719056
- Testing
- Teicoplanin, β-lactams or ciprofloxacin
- Where
- 3 sites in Greece
- Volunteers
- 616 people
- Sponsor
- University of Athens
Osteoarthritis
Blood Management in Orthopedic Surgery
Aim: to investigate whether the use of several transfusion alternatives (erythropoietin, the cell-saver or postoperative drainage and reinfusion systems) in patients undergoing elective total knee or hip replacement surgery can…
- Trial name
- TOMaat (NCT00998088)
- Testing
- erythropoietin and cell saver, erythropoietin, OrthoPAT
- Where
- 4 sites in Netherlands
- Volunteers
- 2,598 people
- Sponsor
- Sanquin Research & Blood Bank Divisions
Hip Fracture, Osteoarthritis
Effectiveness of Two Types of Treatment in Restoring Muscle After Hip or Knee Surgery
The purpose of this study is to determine the effects of two postoperative interventions designed to preserve muscle protein after major hip or knee surgery.
- Conditions
- Hip Fracture, Osteoarthritis, Femur Head Necrosis
- Trial name
- NCT00393848
- Testing
- Essential amino acid supplement, Ketoconazole
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- University of Arkansas
Arthropathy of Knee Joint
Postoperative Pain Management in Hospital and Following Discharge From Hospital.
To investigate postoperative pain management in patients undergoing knee or hip replacement while they are in the hospital and following discharge to their home.
- Trial name
- NCT01907178
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Trinity Health Of New England
Total Knee Replacement Approach, Muscle Torque
Knee Muscle Force Recovery After Minimally Invasive Surgery (MIS) Total Knee Replacement (TKR)
To compare muscle torque recovery between patients under subvastus approach and those under midvastus approach after total knee replacement
- Trial name
- MISTKR (NCT00912769)
- Where
- Taiwan
- Volunteers
- 30 people
- Sponsor
- Far Eastern Memorial Hospital
Total Knee Arthroplasty, Total Knee Replacement
Assessing Function and Pain After Total Knee Arthroplasty With Combined Femoral and Popliteal Nerve Block
The goal of this interventional study is to examine whether a pain management technique of combined femoral and popliteal nerve block is effective in total knee arthroplasty patients.
- Conditions
- Total Knee Arthroplasty, Total Knee Replacement, Total Knee Replacement Surgery, Arthritis Knee
- Trial name
- NCT06196359
- Testing
- Combined Femoral and Popliteal nerve block
- Where
- Israel
- Volunteers
- 34 people
- Sponsor
- University of Haifa
Prosthetic Knee Surgery
Clinical Utility to Follow-up Radiographs During the First Year of Knee Replacement Surgery
Primary prosthetic surgery for the treatment of gonarthrosis is currently one of the most prevalent surgical treatments in Traumatology.
- Trial name
- NCT05944679
- Testing
- No Xray, Xray
- Where
- Spain
- Volunteers
- 200 people
- Sponsor
- Corporacion Parc Tauli
Hip Surgery Corrective, Knee Injuries
Prospective, Randomized Clinical Investigation of Two Different Postoperative Wound Dressings
The primary objective of this investigation is to evaluate if complications related to surgical wound are more common in the treatment group compared to the control group starting from operation day until last visit.
- Trial name
- MxBPo02 (NCT02653183)
- Testing
- Active Comparator: Aquacel Surgical, Experimental: Mepilex Border Post-Op
- Where
- 3 sites in Belgium, Sweden
- Volunteers
- 118 people
- Sponsor
- Molnlycke Health Care AB
Total Knee Arthroplasty, Prosthetic-joint Infection
Methylene Blue in Total Knee Arthroplasty (TKA)
The purpose of this pilot study is to determine the volume of irrigation required to achieve macroscopic clearance of contaminants during a debridement, antibiotics, and implant retention (DAIR) procedure for periprosthetic joint…
- Conditions
- Total Knee Arthroplasty, Prosthetic-joint Infection, Irrigation
- Trial name
- NCT07324954
- Testing
- Methylene Blue 10 MG/ML (intra-articular application), Revision Arthroplasty for PJI (DAIR), Primary Total Knee Arthroplasty
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- University of Miami
Knee Osteoarthritis (OA), Artrosis of the Knee
PROPRIOCEPTION, KINESIOPHOBIA AND FUNCTIONAL RECOVERY AFTER GONARTHROSIS SURGERY
This observational study aims to investigate the relationships between proprioception, causes of kinesiophobia, sensory processing characteristics, and functional recovery in individuals undergoing gonarthrosis surgery.
- Trial name
- NCT07480473
- Where
- Turkey (Türkiye)
- Volunteers
- 47 people
- Sponsor
- Medipol University
Diabetes Mellitus, Type 2, Arthroplasty, Replacement, Hip
CGM Monitoring in T2DM Patients Undergoing Orthopaedic Replacement Surgery
The purpose of this study is to analyze the efficacy and accuracy of real-time continuous glucose monitoring devices (rtCGM) in patients with Type 2 diabetes undergoing inpatient elective hip or knee surgery in the pre-, peri…
- Conditions
- Diabetes Mellitus, Type 2, Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee
- Trial name
- NCT05666479
- Testing
- Dexcom G6 Pro Continuous Glucose Monitor (CGM)
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- Stony Brook University
Pain, Postoperative
Comparison of Fasia Iliac Compartment Block and 4in1 Block
Patients who will undergo elective total knee arthroplasty surgery under spinal anesthesia will be included in the study according to the postoperative analgesia method applied: Group Control, Group FICB and Group 4in1.
- Trial name
- NCT06436105
- Testing
- FICB, 4 in 1 block, Control
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Diskapi Yildirim Beyazit Education and Research Hospital
Venous Thromboembolism
Dose-confirmatory Bridging Study in Total Knee Replacement
The objective of this dose-confirmatory bridging study is to investigate the safety and efficacy of rivaroxaban 5 to 10 mg once-daily (od) dosing in the prevention of venous thromboembolism (VTE) in Japanese patients undergoing…
- Trial name
- NCT01206972
- Testing
- Rivaroxaban (BAY59-7939), Enoxaparin
- Where
- 33 sites in Japan
- Volunteers
- 302 people
- Sponsor
- Bayer
Surgical Wound
A Post-Market Clinical Investigation on Mepilex Border Post-Op
This is a retrospective, observational (non-interventional), single-arm, single-centre, post-market clinical investigation designed to verify clinical performance and safety of Mepilex Border Post-Op when used according to…
- Trial name
- ARCTIS (NCT04994145)
- Where
- Belgium
- Volunteers
- 560 people
- Sponsor
- Molnlycke Health Care AB
Total Knee Arthroplasty Revision, Inflammatory Markers
Fiber Smoothie Supplement
This study aims to assess the feasibility of a 2-week dietary whole-food smoothie intervention and compare outcomes between two groups: patients that integrated a daily whole food plant-based smoothie into their diet for two…
- Conditions
- Total Knee Arthroplasty Revision, Inflammatory Markers, Gut Microbiota
- Trial name
- NCT06896240
- Testing
- Assigned Interventions
- Where
- United States
- Volunteers
- 24 people
- Sponsor
- Hospital for Special Surgery, New York
Total Knee Arthroplasty, Surgical Fear and Worrying
Simulation-Based Preoperative Education in Total Knee Arthroplasty
This randomized controlled trial aims to evaluate the effect of simulation-based preoperative education on surgical fear and kinesiophobia in patients undergoing total knee arthroplasty.
- Conditions
- Total Knee Arthroplasty, Surgical Fear and Worrying, Kinesiophobia
- Trial name
- NCT07310303
- Testing
- Simulation-Based Preoperative Education, Standard Verbal Preoperative Education, Total Knee Arthroplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 48 people
- Sponsor
- Nermin Ocaktan
Degenerative Joint Disease, Osteoarthritis
PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacement.
The objective of this clinical study is to evaluate the operative performance of the PEAK PlasmaBlade 4.0 during total knee replacement; to monitor and record post-operative pain, activity level, narcotic consumption, adverse…
- Trial name
- PRECISE (NCT01081886)
- Testing
- PEAK PlasmaBlade 4.0, Traditional Electrosurgery with scalpel
- Where
- 2 sites in United States
- Volunteers
- 24 people
- Sponsor
- Medtronic Surgical Technologies
Knee Arthroplasty, Total
FactOr XIa inhibiTion for the pRevention of venOus Thromboembolism in Patients Undergoing Total Knee Arthroplasty
This study was to compare the study drug BAY1213790 to existing therapies, i.e. enoxaparin or apixaban, for the prevention of blood clotting and safety in patients undergoing total knee arthroplasty (TKA).
- Trial name
- FOXTROT (NCT03276143)
- Testing
- Enoxaparin, Apixaban, BAY1213790
- Where
- 54 sites in Bulgaria, Canada and 11 more
- Volunteers
- 813 people
- Sponsor
- Bayer