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Fractures, Bone clinical trials

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NCT ID: NCT04324580 Recruiting - Clinical trials for Distal Radius Fracture

Postoperative Immobilization and Physical Therapy Following Volar Locked Plating for Distal Radius Fractures

Start date: June 18, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to see if splinting and formal physical therapy are necessary following surgical fixation (open reduction internal fixation) of distal radius fractures (broken wrist). Currently there is no consensus for post-operative protocol following fixation of distal radius fractures. The decision to splint (late mobilization) and prescribe formal physical therapy vs. not to splint (early mobilization) and use self-guided physical therapy is based on surgeon or institutional preference. The goal of this study is to determine if early mobilization leads to improved outcomes and decreased costs without increasing pain or the loss of hardware fixation.

NCT ID: NCT04323410 Recruiting - Clinical trials for Pediatric Overriding Distal Metaphyseal Radius Fractures

Casting Versus Percutaneus Pinning Treatment of Pediatric Overriding Distal Forearm Fractures

Start date: June 29, 2020
Phase: N/A
Study type: Interventional

This is a randomized controlled trial comparing casting in finger-trap traction without reduction versus closed reduction and percutaneous pin fixation of dorsally displaced, overriding distal metaphyseal radius fractures in under eleven years old children.

NCT ID: NCT04311892 Recruiting - Hip Fractures Clinical Trials

Hip Abductor Muscle Dysfunction After Nailing of Proximal Femoral Fractures, Incidence and Contributing Factors.

Start date: January 18, 2019
Phase:
Study type: Observational

Proximal femoral fractures(PFFs) are common with advancing age. Proximal femoral nail (PFN) is now increasingly used to fix unstable fractures. Studies have demonstrated that muscle strength deficit is significantly large after PFFs. N. Ivanova et al found that hip muscle isometric strength for the fractured leg was significantly decreased 1 week and 6 months postoperatively. Besides, a recent study done by Nitin Wale et al concluded that abductor weakness and trendeleburg gait are fairly common in patients treated with PFN and this complaint is often overlooked. Despite significant improvement in muscle function after at least 6 months of physiotherapy as demonstrated by previous studies, we didn't come over a study explaining the main causes of remaining abductor lurch in patients with united fracture of the proximal femur treated using proximal femoral nail (short type).

NCT ID: NCT04309539 Recruiting - Clinical trials for Proximal Femur Fracture

Which Analgesia is Better for Proximal Femoral Fractures?

Start date: September 21, 2020
Phase: N/A
Study type: Interventional

This patient population is typically elderly and frail. They are at risk of adverse effects secondary to inadequate pain management such as prolonged admissions and poor functional outcomes. Regional analgesia is preferred due to their opioid-sparing effects and reduction in related adverse effects but The analgesia from these blocks is only moderate and literature suggests that the obturator nerve (ON) is not covered.

NCT ID: NCT04307342 Recruiting - Humerus Fracture Clinical Trials

Posterior Minimally Invasive Plate Osteosynthesis (MIPO) for Humerus Diaphyseal Fractures

MIPOH
Start date: July 1, 2018
Phase:
Study type: Observational [Patient Registry]

The primary objective is to evaluate the clinical, functional and radiological results in patients treated with posterior MIPO for Humerus Diaphyseal Fractures With Extra-articular Distal Humeral Anatomical Plate.

NCT ID: NCT04306536 Recruiting - Femur Fracture Clinical Trials

Nutritional Support in Femur Fracture Rehabilitation

Start date: June 19, 2020
Phase: N/A
Study type: Interventional

This randomized, observer-blinded trial tested the hypothesis that nutritional supplementation with muscle-target nutritional supplementation would increase the efficacy of a physical rehabilitation program in old adults with femur fracture treated with surgery.

NCT ID: NCT04299022 Recruiting - Fractures, Bone Clinical Trials

Safety, Efficacy, & Use of ViviGen Cellular Bone Matrix Allograft in Orthopaedic Fracture Care

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

Prospective registry and retrospective data collection study to assess the efficacy and safety of Vivigen Cellular Bone Matrix (Vivigen) in orthopaedic trauma patients who require bone grafting in the acute, delayed, non-union fracture as well as use in fusion procedure settings.

NCT ID: NCT04274530 Recruiting - Pain, Postoperative Clinical Trials

Cognitive Behavioural Therapy to Optimize Post-Operative Recovery Trial

COPE
Start date: January 25, 2021
Phase: N/A
Study type: Interventional

Psychological factors such as stress, distress, anxiety, depression, and poor coping strategies may be associated with ongoing pain following injuries such as fractures. To study this relationship, patients will undergo cognitive behavioural therapy (CBT) which is designed to modify such thoughts with the goal of reducing ongoing pain and improving quality of life. The goal of this study is to determine if CBT, versus usual care, reduces the prevalence of moderate to severe persistent post-surgical pain (PPSP) over 12-months post-fracture in patients with an open or closed fracture of the appendicular skeleton, treated with internal fixation.

NCT ID: NCT04250415 Recruiting - Clavicle Fracture Clinical Trials

Multi-Center Adolescent Clavicle Fracture Trial: Operative vs. Non-Operative Treatment

FACTS
Start date: March 11, 2013
Phase:
Study type: Observational [Patient Registry]

Investigators from eight tertiary care, level 1 pediatric trauma centers have developed a protocol for the establishment of a formal, prospective multi-center adolescent clavicle registry, with designs for standardized radiographic assessment and the prospective collection of validated outcome measures and complications data, for all patients, ages 10-18, treated for clavicle shaft fractures, operatively and non-operatively. Eventually, the investigators would like to do comparative analysis for the operative and non-operative treatment arms, with additional sub-stratified analyses performed within these treatment arms by age and activity level. Among the primary goals of research projects stemming from the first arm of this registry, FACTS A, is to explore the hypothesis that non-operative treatment is associated with lower costs, greater safety, and equivalent or superior outcomes, compared with operative treatment, despite a national trend towards increasing surgical treatment. The second arm of the registry, FACTS B, will continue to investigate the same hypotheses, excluding cost outcomes, in patients only with completely displaced midshaft clavicle fractures.

NCT ID: NCT04247295 Recruiting - Bone Fracture Clinical Trials

Comparison of Woodcast vs Traditional Cast in Distal Radius Fracture

Start date: December 7, 2017
Phase: N/A
Study type: Interventional

The investigators project is a randomised controlled trial that will compare the efficacy of the traditional casting method against the woodcast splint in distal radial fracture. After the investigators have taken consent and the patients have agreed to be a part of the project, the investigators will randomly divide the participants into two groups. One with the traditional cast and one with the wood cast. The difference will be measured by using the EQ-5D-Y tool alongside the use of the DASH score and our own questionnaire. The study will take place over the following year with the Sheffield Children's Hospital being the only site involved. Woodcast products have the CE declaration of conformity which is covered for the use in children, and apart from the type of cast the child is given, the course of treatment is the same for both group