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Radius Fractures clinical trials

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NCT ID: NCT04359017 Withdrawn - Pediatrics Clinical Trials

Systemic Absorption of Lidocaine After Hematoma Block

Start date: November 1, 2020
Phase: Phase 4
Study type: Interventional

This study will measure in children how much numbing medicine, lidocaine, is absorbed into the bloodstream after it is injected into a blood clot (hematoma) around a forearm fracture for pain control when the broken bone is moved back into place (fracture reduction). This is called a hematoma block and is commonly used in the Emergency Unit. To help with anxiety and to add additional pain control, nitrous oxide (laughing gas) is given while the lidocaine hematoma block is placed and continued during the fracture reduction. Advantages of using this technique for pain control instead of an intravenous anesthetic such as ketamine include faster recovery and discharge home, and longer pain control. Of concern, if too much lidocaine is absorbed into the bloodstream, seizures and irregular heart beating may occur. Bloodstream concentrations of lidocaine after a hematoma block have been measured in only one study of 8 adults and found to be at significant but safe levels. No study has been published in children to measure bloodstream lidocaine levels when a hematoma block is used. Because children's bones are still growing and more metabolically active than adult bones, the investigators believe it is important to determine whether lidocaine blood levels in children are also at safe levels when using a standard lidocaine hematoma block for reduction of fractures. The investigators also want to determine whether bloodstream lidocaine levels correlate with type of fracture. The investigators also aim to determine if there is a difference in absorption pattern between different types of distal radius fractures, if there is a correlation between fracture type and systemic lidocaine absorption, and if there is a correlation between fracture type and ability to provide adequate pain and sedation control with lidocaine hematoma block/inhaled nitrous combination. The investigators believe blood lidocaine levels after hematoma block in children will peak at safe levels, but will be higher than those observed in adults.

NCT ID: NCT04135768 Withdrawn - Clinical trials for Radius Fracture Distal

A Study Examining The Effect Of Wrist Joint Haematoma Washout As An Adjunct Procedure To Plating Of The Distal Radius In Fractures Of The Distal Radius Involving The Wrist Joint

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

Intra-articular fractures of the distal radius are common in urban populations and result in significant morbidity in terms of time away from work. Volar plating of the distal radius is a commonly used mode of surgical fixation of this fracture. The joint haematoma resulting from the fracture has been hypothesized to contribute to the post-injury disability. As such, this study aims to examine if the evacuation of the haematoma during volar plating results in superior functional outcomes at three months post surgery.

NCT ID: NCT03779958 Withdrawn - Clinical trials for Carpal Tunnel Syndrome

Alternatives to Hand Therapy for Hand Surgery Patients

Start date: January 12, 2019
Phase:
Study type: Observational

Patients will be asked to use a mobile phone app to conduct their hand therapy after having hand surgery.

NCT ID: NCT02093364 Withdrawn - Clinical trials for Failed Open Reduction Internal Fixation (ORIF) of a Radial Head Fracture

A Focused Registry to Document the Use of the Short- or Long-stemmed Radial Head Prosthesis (RHP)

Start date: July 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this focused registry is to evaluate the clinical implications of the RHP position (relative to the articulations) regarding functional and radiographic parameters in patients treated with the RHP with a straight and curved stem.

NCT ID: NCT00788190 Withdrawn - Clinical trials for Distal Radius Fractures

Treatment of Distal Radius Fractures in Elderly Patients

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

The purpose of this study is to create and test a treatment algorithm to guide the treatment of distal radius fractures in patients 65 and older and to obtain level-one evidence to determine the best method of treating distal radius fractures in this growing population demographic.