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Femoral Neck Fractures clinical trials

View clinical trials related to Femoral Neck Fractures.

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NCT ID: NCT04589598 Recruiting - Clinical trials for Femoral Neck Fractures

Femoral Neck System and Multiple Cannulated Screws in Femoral Neck Fracture

Start date: October 30, 2019
Phase: N/A
Study type: Interventional

Investigators will compare the clinical outcomes of femoral neck system with conventional multiple cannulated screw in non-displaced femoral neck fracture.

NCT ID: NCT04577261 Recruiting - Clinical trials for Femoral Neck Fractures

FNS (FEMORAL NECK SYSTEM) Study

FNS
Start date: October 7, 2020
Phase:
Study type: Observational

A post-market, prospective study to evaluate the reoperation rate of displaced and nondisplaced femoral neck fractures treated with the Femoral Neck System (FNS)™

NCT ID: NCT04462172 Recruiting - Clinical trials for Femoral Neck Fractures

A Prospective Multicenter Cohort Study About Internal Fixation Using FNS Versus MCS for Femoral Neck Fracture

Start date: September 30, 2021
Phase: N/A
Study type: Interventional

This prospective multicenter cohort study is to compare the post-operative implant failure rate between the patients with femoral neck fracture (AO classification 31-B) using Femoral Neck System (FNS) versus Multiple Cancellous Screws (MCS) at 2-year follow up. The patients are divided into the FNS group and the MCS group according to the internal fixation they choose. The internal fixation failure rate (IFFR) and differences in fracture prognosis of the two groups will be compared. Obtain clinical data of FNS in the Chinese population, and verify the safety and efficacy of FNS for patients with femoral neck fracture.

NCT ID: NCT04349046 Recruiting - Clinical trials for Rheumatoid Arthritis

Exception Cementless Hip Stem

Exception
Start date: January 1, 2021
Phase:
Study type: Observational

This study is a multicenter, retrospective and prospective, non-controlled, non-randomized post market clinical follow-up study. The objectives of this study are to confirm the long-term safety, performance and clinical benefits the Exception Cementless femoral stem (standard and varized) when used in primary total hip arthroplasty.

NCT ID: NCT04017403 Recruiting - Knee Osteoarthritis Clinical Trials

Probiotics Attenuate Postoperative Cognition Decline

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate whether perioperative probiotics can reduce the incidence of postoperative cognitive dysfunction and postoperative delirium.

NCT ID: NCT03966716 Recruiting - Clinical trials for Femoral Neck Fractures

Hips Screws or (Total) Hip Replacement for Undisplaced Femoral Neck Fractures in Elderly Patients (HipSTHeR)

HipSTHeR
Start date: September 16, 2019
Phase: N/A
Study type: Interventional

A registerbased RCT will investigate whether arthroplasty can decrease the reoperation rate compared to internal fixation for patients with an undisplaced femoral neck fracture (Garden I-II).

NCT ID: NCT03909815 Recruiting - Clinical trials for Femoral Neck Fractures

Dual Mobility Cups in Hip Fracture Patients

DUALITY
Start date: January 17, 2020
Phase: N/A
Study type: Interventional

Our aim is to develop a strategy that reduces the risk of dislocations after total hip arthroplasty surgery performed due to femoral neck fracture. We therefore perform a register-nested, pragmatic, randomized controlled trial to investigate the safety and efficacy of dual mobility cups that were designed to minimize the risk of dislocation in the large and fragile group of elderly patients with femoral neck fractures.

NCT ID: NCT03550079 Recruiting - Clinical trials for Femoral Neck Fracture

Fixation for the Treatment of Femoral Neck Fractures

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The femoral neck fracture is the most prevalent injuries which commonly encountered among older people with high mortality, morbidity and young fit healthy ones who subjected to high-energy trauma . Non-union or avascular necrosis of femoral neck fracture which lead to loss of labor capacity and death, is the most commonly occurred complication and results in considerable burden for family. The treatment is difficult and challenging, and to minimize the negative results such as limited mobilization or other complications, it is essential to take active prevention and appropriate treatment depending on fracture pattern and patients' characteristics as early as possible. However, current implant selections for femoral neck fractures remain a topic of greater interest and controversy, and vary substantially from each other .

NCT ID: NCT02877472 Recruiting - Clinical trials for Femoral Neck Fracture

Porous Tantalum Rods Improve the Hip Joint Function of Patients With Avascular Necrosis of the Femoral Head

Start date: May 2015
Phase: N/A
Study type: Interventional

To confirm 1) whether, compared with core decompression alone, core decompression with porous tantalum rod implantation improves the hip joint function of patients with avascular necrosis of the femoral head after femoral neck fracture surgery, 2) whether porous tantalum rod shows favorable biocompatibility with the human body, and 3) whether this treatment method is feasible for treating avascular necrosis of the femoral head after femoral neck fracture surgery.

NCT ID: NCT02783274 Recruiting - Clinical trials for Rheumatoid Arthritis

Actis Total Hip System 2 Year Follow-up

Actis14014
Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Two-year (2 year) information regarding the performance of the commercially available Actis™ Total Hip System in order to obtain and evaluate the clinical outcomes on a series of cementless primary total hip arthroplasty (THA) and hemi-hip arthroplasty procedures using clinical, radiographic and device and procedure related adverse event assessments.