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Periprosthetic Fractures clinical trials

View clinical trials related to Periprosthetic Fractures.

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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: 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: 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.

NCT ID: NCT02854566 Completed - Clinical trials for Periprosthetic Fracture of the Femur

Periprosthetic Fractures of the Femur Treated by Osteosynthesis

Start date: June 2016
Phase:
Study type: Observational

Observational retrospective study on 36 consecutive patients having had surgery for a periprosthetic fracture of the femur between 2010 and 2015. The goal of the study is to test whether osteosynthesis was a secure choice at a certain age and with any type of Vancouver fracture.

NCT ID: NCT02391129 Completed - Clinical trials for Periprosthetic Fractures

Locking Compression Plate Fixation Versus Revision- Prosthesis of Vancouver-B2, B3 and C Periprosthetic Femoral Fractures After Total Hip Replacement

Start date: January 2014
Phase: N/A
Study type: Observational

The purpose of this study was to compare the clinical (range of motion, weight bearing, quality of life) and radiographic outcome (boney consolidation) between open reduction and internal fixation using locking compression plates with revision prosthesis using a non-cemented long femoral stem in a group of patients with a Vancouver type-B2, B3 and C periprosthetic fracture after primary total hip replacement.