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Fractures, Bone clinical trials

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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: NCT03906032 Recruiting - Hip Fractures Clinical Trials

Comparison of Sliding Hip Screw to Intra Medullary Nailing in the Treatment of Intertrochanteric Hip Fracture

Start date: April 2, 2019
Phase: N/A
Study type: Interventional

Shortening of the abductor lever arm is a particular concern with the SHS, and the resultant biomechanical alterations impairs gait, including decreased cadence and increased double support time on the injured side. The use of a IM nail device may stop this shortening and improve functional parameters in this patient cohort

NCT ID: NCT03903510 Recruiting - Fractures, Bone Clinical Trials

Virtual Reality During Pediatric Cast Removal

Start date: May 21, 2019
Phase: N/A
Study type: Interventional

This study is a randomized control trial of Virtual Reality during cast removal procedures at a pediatric tertiary care center.

NCT ID: NCT03899025 Recruiting - Scaphoid Fracture Clinical Trials

Diagnostics of Scaphoid Fractures With HRpQCT

Start date: December 12, 2017
Phase: N/A
Study type: Interventional

The scaphoid bone is the most common fractured carpal bone. Scaphoid fractures represent 2-6% of all fractures and occur mainly in young, active patients aged 15 to 40. The scaphoid bone has an essential role in functionality of the wrist, acting as a pivot. Correct treatment of a scaphoid fracture depends on accurate and timely diagnosis, and inadequate treatment can result in avascular necrosis (up to 40%), nonunion (5-21%) and early osteoarthritis (up to 32%) that may seriously impair wrist function. In addition, impaired consolidation of scaphoid fractures results in longer immobilization leading to significant functional and psychosocial impairment thus having considerable socio-economic consequences and negative impact on the quality of life. Current diagnostic pathways can take up to two weeks to diagnose (or exclude) a scaphoid fracture, leading to overtreatment in patients with a suspected scaphoid fracture since only 15 to 30% of suspected scaphoid fractures in the Netherlands annually is found to be an actual fracture. Thus, there is significant room for improvement in the diagnostic pathway of scaphoid fractures.

NCT ID: NCT03898154 Recruiting - Clinical trials for Distal Radius Fracture

Perioperative Glucocorticoid Administration in the Treatment of Adult Distal Radius Fractures

Start date: July 10, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this investigation is to compare functional outcome measures and range of motion for patients receiving glucocorticoid (GC) injections versus those not receiving GCs for the treatment of distal radius fractures. The investigators hypothesize that patients who receive GC will have improved ROM and functional outcome measures compared to patients who do not receive GC. In addition, this study aims to determine if there is a difference in rates of complications and postoperative pain control between the GC and non-GC groups. In order to accomplish these aims, the investigators will conduct a prospective, randomized, controlled investigation.

NCT ID: NCT03891888 Recruiting - Tibial Fractures Clinical Trials

Intramedullary Bone Grafting for Open Tibial Shaft Fractures

Start date: March 26, 2020
Phase: N/A
Study type: Interventional

This study will examine if there is a difference between the time to full union between the control group and the study group. Each group will be composed of patients who have an open fracture in the mid tibia. Both groups will undergo primary fixation via reamed intramedulary nailing (IMN), a common treatment for tibia shaft fractures in adults. The study group will have a bone graft applied to the open cortex of the fracture. The bone graft will be composed of the intramedullary reamings, which are a byproduct produced when the intramedullary canal is reamed in preparation for insertion of the IMN.

NCT ID: NCT03887988 Recruiting - Orbital Fractures Clinical Trials

Orbital Fractures Registry

OFx
Start date: November 1, 2019
Phase:
Study type: Observational [Patient Registry]

Approximately 300 patients presenting orbital blow-out fracture will be enrolled prospectively in this registry. All patients, surgically and nonsurgically treated as per standard (routine) of care will be followed-up (FU) within the registry for a period of 6 months.

NCT ID: NCT03871322 Recruiting - Fracture Healing Clinical Trials

The Vitamin K2 and D3 Intervention Trial in Children and Adolescents With the Low-energy Fractures

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

a prospective, three- month, randomized, double-blind, placebo-controlled, intervention trial (RDBPC), investigating the effect of vitamin K2 (menaquinone-7) and vitamin D3 on the healing process of low-energy bone fractures in children and adolescents

NCT ID: NCT03868280 Recruiting - Femur Fracture Clinical Trials

The FLiP Study, a Pilot Cluster Randomized Trial

FLiP
Start date: October 16, 2020
Phase: N/A
Study type: Interventional

The primary objective of this pilot trial is to assess the feasibility of a definitive trial to determine the effect of lateral patient positioning versus supine positioning with fracture table use for reamed antegrade intramedullary fixation of femur fractures.

NCT ID: NCT03856450 Recruiting - Clinical trials for Distal Radius Fracture

Use of Digital Tomosynthesis for Detection and Case Management of Scaphoid and Distal Radius Fractures: A VolumeRAD Data Collection Study

Start date: December 20, 2018
Phase: N/A
Study type: Interventional

The study described herein is being conducted to collect clinical data associated with diagnosis and treatment information using the VolumeRAD advanced application.