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Radius Fractures clinical trials

View clinical trials related to Radius Fractures.

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NCT ID: NCT03056950 Recruiting - Rehabilitation Clinical Trials

BFR DISTRAD NON OP: Blood Flow Restricted Training During Rehabilitation Following Distal Radius Fracture

Start date: March 2016
Phase: N/A
Study type: Interventional

Occlusion training, resistance exercise performed with a specialized venous tourniquet, leads to beneficial changes in muscle strength at low resistance and minimal stress on the nearby joint. This novel resistance training has the potential to greatly improve muscle strength gains in individuals who are unable, for medical reasons, to perform the high resistance exercises typically required to improve strength. Our study will examine the effect of this technique on strength recovery following distal radius fracture treated with cast immobilization (non-operatively). The primary objective of the intervention is to achieve accelerated recovery of forearm, wrist and hand function as assessed using measures such as grip/pinch strength, validated questionnaires, and functional outcome testing. Occlusion training can potentially serve as a specialty intervention for rehabilitation patients, reduce the cost of care, and improve the treatment options for both patients and providers.

NCT ID: NCT03048214 Completed - Acute Pain Clinical Trials

Effect of Nerve Block Versus General Anaesthesia for Distal Radial Fracture Surgery

Start date: May 16, 2017
Phase: N/A
Study type: Interventional

This study aims to investigate whether infraclavicular nerve block improves acute postoperative pain after distal radial fracture surgery.

NCT ID: NCT03014024 Completed - Colles' Fracture Clinical Trials

Low-level Laser Therapy in Distal Radius Fractures

Start date: December 2016
Phase: N/A
Study type: Interventional

Conservative treatment of distal radius fracture is immobilisation with cast for 4-6 weeks. After removing the cast, it is common to still have pain, swelling and reduced mobility in the wrist. The aim of this study is to evaluate the influence of LLLT on the hand.

NCT ID: NCT03011905 Completed - Pain, Postoperative Clinical Trials

Rebound Pain After Operations for Distal Radius Fractures With a Volar Plate in Brachial Plexus Block

Start date: January 2017
Phase: Phase 3
Study type: Interventional

Many patients have strong pain at brachial plexus block resolution after operations for distal radius fractures with a volar plate. This study investigates if a single dose of dexamethasone in addition to a standard pain regime have an effect on postoperative pain. The primary endpoint is difference in the highest pain score first 24 hours after surgery. The investigators will also look at pain scores and analgesics consumption first few hours after surgery and at different times up to 2 years after surgery.

NCT ID: NCT03009890 Completed - Clinical trials for Radius Distal Fracture

Surgery vs. Casting for Displaced Articular Radius Fractures in Elderly

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

Objective: to compare the functional outcome after open reduction and internal fixation with non-operative cast treatment for elderly patients with displaced intra-articular distal radius fractures.

NCT ID: NCT02990052 Completed - Clinical trials for Distal Radius Fractures

Conservative Treatment vs. Volar Plating of Distal Radius Fractures

DRF
Start date: November 2008
Phase: N/A
Study type: Interventional

A prospective, randomized controlled single-center trial with 80 patients aged 50 years and above to compare the functional and radiological results of conservative treatment and volar fixed-angle plating in the management of distal radius fracture

NCT ID: NCT02962206 Recruiting - Clinical trials for Point-of-care Ultrasound, Distal Radius Fracture

The Effect of Point-of-care Ultrasound Guidance for Distal Radius Fracture Reduction

Start date: January 10, 2017
Phase: N/A
Study type: Interventional

Distal radius (Colle's) fractures in adult patients are commonly reduced in the emergency department before casting. Standard of care currently requires that x-rays be performed before and after fracture reduction, and inadequate reductions may be subject to repeat attempts and are at a higher risk to require surgery. This study will assess the use of point-of-care ultrasound (POCUS) in addition to standard care as a tool to decrease the angulation at the fracture site after a reduction is performed. If this angulation is decreased, it would suggest that POCUS for distal radius fracture reduction could decrease the number of failed reduction attempts and therefore the number of repeated reduction attempts.

NCT ID: NCT02957240 Recruiting - Clinical trials for Musculoskeletal Pain

Graded Motor Imagery for Women at Risk for Developing Type I CRPS Following Closed Treatment of Distal Radius Fractures

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Nearly 2 out of 10 women will sustain a distal forearm fracture throughout their lifespan.Recent longitudinal studies illustrate that as many as 1/3 of all persons who undergo closed reduction and casting for distal radius fractures (DRF) go on to develop type 1 complex regional pain syndrome (CRPS). Graded motor imagery (i.e., motor imagery and mirror therapy), a movement representation technique, is strongly supported in the literature as a treatment of CRPS and has recently been suggested as a potential strategy to prevent its onset. Other complications include disability, wrist/forearm tightness and sensorimotor changes. The investigators propose that an early intervention protocol which includes graded motor imagery (GMI) will improve the pain, functional and upper limb sensorimotor outcomes of persons following closed reduction and casting of DRF relative to a standard of care intervention.

NCT ID: NCT02909647 Recruiting - Clinical trials for Distal Radius Fracture

Three Dimensional Digital Preoperative Planning for the Osteosynthesis of Distal Radius Fractures

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

Background: Three dimensional (3D) digital pre-operative planning software for osteosynthesis of fractures was developed. To assess the usefulness of the 3D planning, we evaluated the accuracy of the reduction shapes and selected implants in the patients with distal radius fractures. Methods: Thirty wrists of 30 distal radius fracture patients who underwent osteosynthesis using volar locking plates were evaluated. Fifteen wrists were treated with 3D preoperative planning as the plan group. The other fifteen wrists were treated with conventional preoperative planning as the control group. Volar tilt and radial inclination were measured after operation and compared with the healthy side wrist. In addition, preoperative planning and postoperative reductions were compared by measuring the volar tilt and radial inclination of the 3D images in the plan group. The intra-class correlation coefficient (ICC) values of the radiological parameters between healthy side wrists and injured side wrists, between preoperative planning and postoperative reductions were evaluated. For the accuracy of the implant choices, the ICCs for the screw lengths between the preoperative plan and the actual choices were evaluated in the plan group.

NCT ID: NCT02894983 Completed - Clinical trials for Distal Radius Fracture

Conservative Treatment of Distal Radius Fracture in Elderly in Randomized Controlled Trial

Start date: June 2016
Phase: N/A
Study type: Interventional

There is no consensus about the best conservative treatment for patients with dorsally displaced distal radius fractures. The previous studies that have examined the most valid method for cast immobilization have lacked uniform and patient-rated outcome measures, proper randomization and sufficient study population. The aim of this study is to compare functional position cast to flexion-ulnar -deviation with dorsally displaced distal radius fractures in patients aged 65 years or older. The conservative treatment is performed in clinical practice by various health care professionals with different techniques of reduction which are not limited to any specific technique in this pragmatic, randomized controlled trial.