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Fractures, Bone clinical trials

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NCT ID: NCT04349319 Recruiting - Clinical trials for Distal Humerus Fracture

Development of Three Dimensional Preoperative Planning System for the Osteosynthesis of Distal Humerus Fractures

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

To reproduce anatomical reduction and appropriate implant placement/choices during osteosynthesis for elbow fractures, a 3D preoperative planning system was developed. To assess the utility of 3D digital preoperative planning for the osteosynthesis of distal humerus fractures, the reproducibility of implant reduction shapes and placements in patients with distal humerus fractures will be evaluated.

NCT ID: NCT04343118 Completed - Clavicle Fracture Clinical Trials

Benefit of Surgical Hardware Removal Following Clavicle Fracture

Start date: January 1, 2015
Phase:
Study type: Observational

Little is known about the beneficial aspects of elective implant removal following plate osteosynthesis of displaced clavicle fractures.

NCT ID: NCT04335461 Withdrawn - Pain, Postoperative Clinical Trials

Postop Pain Control in Hip Fracture Surgery: Fascia Iliaca Compartment Block Versus Fracture Block

Start date: August 5, 2021
Phase: Early Phase 1
Study type: Interventional

The investigators propose to investigate the effect of intraoperative FICB and intrafragmentary fracture blockade on postoperative pain and opiate consumption using a randomized controlled trial study design. There will be three treatment groups: (1) fascia iliaca compartment blockade administered after surgical fixation using the loss of resistance technique with 30cc 0.25% marcaine (2) intrafragmentary fracture block using fluoroscopy guidance after surgical fixation with 30cc 0.25% marcaine and (3) placebo group, with no intervention.

NCT ID: NCT04332497 Withdrawn - Clavicle Fracture Clinical Trials

Clavipectoral Fascia Plane Block Versus Interscalen Brachial Plexus Block for Clavicle Surgery

Start date: April 10, 2020
Phase: N/A
Study type: Interventional

The pain after clavicle fracture surgery may be managed with combined superficial cervical plexus-interscalene block and recently clavipectoral fascia plane block (CPB). CPB was defined by Valdes in 2017 firstly. It may be used for postoperative analgesia after clavicle surgery. CPB may be an alternative to interscalene brachial plexus block. The aim of this study is to compare the efficacy of the US-guided CPB and ISCB for postoperative analgesia management after clavicle surgery. The primary aim is to compare perioperative and postoperative opioid consumption and the secondary aim is to evaluate postoperative pain scores (VAS), adverse effects related with opioids (allergic reaction, nausea, vomiting).

NCT ID: NCT04332159 Recruiting - Pain, Acute Clinical Trials

Inhaled Methoxyflurane for Pain Management in Nasal Bone Fracture Reduction

Start date: October 10, 2019
Phase: Phase 3
Study type: Interventional

This is a randomised, double-blind, placebo controlled study to evaluate the efficacy of Methoxyflurane (Penthrox®) for the treatment of acute pain during closed nasal fracture reduction. The study aims to provide evidence under blinded controlled conditions that Penthrox is safe and effective in patients aged 18 to 65 years during closed nasal fracture reduction.

NCT ID: NCT04328558 Withdrawn - Clavicle Fracture Clinical Trials

Clavipectoral Fascia Plane Block for Clavicle Surgery

Start date: April 22, 2020
Phase: N/A
Study type: Interventional

The pain after clavicle fracture surgery may be managed with combined superficial cervical plexus-interscalene block and recently clavipectoral fascia plane block (CPB). CPB was defined by Valdes in 2017 firstly. It may be used for postoperative analgesia after clavicle surgery. CPB may be an alternative to interscalene brachial plexus block. The aim of this study is to evaluate the efficacy of the US-guided CPB for postoperative analgesia management compare to no intervention control group after clavicle surgery. The primary aim is to compare postoperative opioid consumption and the secondary aim is to evaluate postoperative pain scores (VAS), adverse effects related with opioids (allergic reaction, nausea, vomiting).

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: NCT04311866 Withdrawn - Pediatric ALL Clinical Trials

Femoral Pediatric Fractures. Walking Spica Cast vs Synthetic Pants

Start date: January 4, 2020
Phase: N/A
Study type: Interventional

Femoral pediatric shaft fractures are a common orthopedic injury. Conservative treatment is still the preferred method by orthopedic surgeons. The walking spica cast is used in patients between 1 year old and 6 years old, in patients with isolated and low-energy fractures. The use of synthetic materials is preferred (fiber glass) for resistance, durability and low weight makes them optimal.