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Periprosthetic Fractures clinical trials

View clinical trials related to Periprosthetic Fractures.

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NCT ID: NCT06028971 Recruiting - Clinical trials for Distal Femur Fracture

Safety and Performance of the Biphasic Plate Distal Femur: A Multicenter Case Series

Start date: January 30, 2024
Phase:
Study type: Observational

The goal of this observational multicenter case series is to assess the safety and performance of the CE-marked "Biphasic Plate Distal Femur" during standard of care.

NCT ID: NCT05805774 Recruiting - Clinical trials for Distal Femur Fracture

pDIFFIR: Geriatric Periprosthetic DIstal Femur: FIxation Versus Replacement

pDIFFIR
Start date: February 1, 2024
Phase: N/A
Study type: Interventional

Periprosthetic distal femur fractures are a significant source of morbidity and mortality for elderly patients. One treatment option involved a surgical fixation with plates or nails, screws and cables/wires along the side of your fractured bone. The second method consists in replacing your knee joint with an artificial knee prosthesis (artificial knee joint). The primary objective is to determine if acute distal femur replacement improves knee pain and functional outcomes compared to surgical fixation. Secondary outcomes are mortality, reoperation, complications, post-operative pain and quality of life. A health economic analysis will be conducted to assess the cost-effectiveness of both treatments. A total of 148 patients (74/group) will be enrolled in the study.

NCT ID: NCT05697965 Not yet recruiting - Clinical trials for Arthroplasty Complications

LocalVancomycinPowderToPreventPeriprostheticJointInfection.

Start date: March 1, 2023
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and complication profile of local vancomycin application in primary arthroplasty. The investigators hypothesized that the use of local antibiotics would decrease the rate of infection compared to controls and this will be achieved by applying 1 gm of vancomycin powder intracapsularly.

NCT ID: NCT04833634 Completed - Clinical trials for Periprosthetic Fracture Around Prosthetic Joint Implant

Follow-Up of the Prevision® Hip Stem

PRESPECT
Start date: May 14, 2021
Phase:
Study type: Observational

The main objective of this study is to represent the treatment reality at the study site and to draw conclusions from cases of failure or suboptimal outcome. Potential risk factors for revision surgery, suboptimal outcome or radiologic sign of loosening, bone non-union or stem subsidence will be evaluated. Next to the functional outcome, stem subsidence will be used as an important indicator for a stable fixation of the revision stem.

NCT ID: NCT04663893 Recruiting - Clinical trials for Periprosthetic Fractures

Peri-Implant and Peri-Prosthetic Fractures: Epidemiology, Morbidity, Mortality, Treatment and Outcome Analysis

PIPPAS
Start date: January 1, 2021
Phase:
Study type: Observational [Patient Registry]

This study supports Spanish data collection and analysis on Periprosthetic and Peri-implant fractures of the upper and lower limb. Treatment and clinical management of this fractures are complex and goes along with complications. There will be more than 70 hospitals providing information. This study will provide evidence on which is the best treatment for every unique patient. This will help trauma surgeons and geriatricians to provide better treatments, to improve health care in our society, reducing mortality, morbidity, improving functional outcomes, and reducing costs, which in turn will be advances in trauma care.

NCT ID: NCT04367272 Not yet recruiting - Clinical trials for Osteoarthritis, Knee

Is Second Knee at Risk During Simultaneous Bilateral Total Knee Arthroplasty.

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

The effects of single-team simultaneous bilateral total knee arthroplasty on peri- and postoperative complications are clear. The investigators hypothesized that second knee at risk during single-team simultaneous bilateral total knee arthroplasty and have more early postoperative complication rates than the first knee. Therefore, this prospective study compared minor and major local complications for 90 days postoperatively between the first and second during knee single-team simultaneous bilateral total knee arthroplasty.

NCT ID: NCT03622346 Completed - Cystic Echinococcus Clinical Trials

Periprosthetic Fracture Following Tibial Echinococcosis

Start date: January 5, 2010
Phase: N/A
Study type: Interventional

Cystic Echinococcus in the bone is rare, comprising 0.5% to 2.5% of all human hydatidosis Association of Hydatid disease to pathologic fractures involving knee prosthesis have not yet been described A combined surgical and medical approach is of paramount importance to avoid recurrence Resulting osseus defects is challenging and require specific prosthesis when treating this entity.

NCT ID: NCT03378557 Recruiting - Clinical trials for Periprosthetic Fractures

Periprosthetic Fracture Registry (PPFx)

PPFx
Start date: December 31, 2018
Phase:
Study type: Observational [Patient Registry]

This registry supports international data collection and research on PPFx treatments after hip and knee arthroplasty. A registry such as this ultimately aims to provide far-reaching benefits to society including reduced morbidity and mortality, improved patient safety, improved quality of care and medical decision-making, reduced medical spending, and advances in orthopaedic science.

NCT ID: NCT03358186 Not yet recruiting - Clinical trials for Periprosthetic Fractures

Investigation on the Surgical Treatment Effect of Periprosthetic Femur Fracture After Hip Arthroplasty

Start date: March 1, 2018
Phase: N/A
Study type: Observational

To Investigate the Surgical Treatment effect of Periprosthetic Femur Fracture After Hip Arthroplasty

NCT ID: NCT03326271 Completed - Clinical trials for Femoral Neck Fractures

Postoperative Periprosthetic Fractures in Hip Fracture Patients: Exeter vs Anatomic SP2 Lubinus Stem

PPFEvL
Start date: May 4, 2016
Phase:
Study type: Observational

Recent studies have indicated a high incidence of postoperative periprosthetic femoral fracture in elderly patients treated with two commonly used cemented polished, tapered femoral stems. The aim of this study was to compare the prevalence and incidence rate of PPF in a cohort of elderly with femoral neck fractures (FNF) treated with either a collarless, polished, tapered stem (Exeter) or an anatomic matte stem (Lubinus SP 2). Patients and Methods In a multicentre retrospective cohort study 2529 patients 60 years and above, with a FNF as indication for primary surgery with a cemented hip arthroplasty were included. Patients were treated either with a polished tapered Exeter stem or a matte anatomic Lubinus SP12 stem according to the surgeons preference or to the praxis of the present department. The incidence of perprosthetic femoral fractures Hip-related complications and repeat surgery were assessed at a minimum follow-up of 2 years postoperatively.