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Hand Injuries clinical trials

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NCT ID: NCT04930718 Not yet recruiting - Pain, Chronic Clinical Trials

Thumb and Wrist Proprioception Exercises.

Start date: June 15, 2021
Phase: N/A
Study type: Interventional

Distal radius fracture is the most common upper extremity fracture with peak incidence among older women after the fifth decade of life. Proprioception is one constituent of a complex Sensory motor control process. Proprioception requires the reception and central integration of incoming afferent signals. Although various sensory and motor deficits have been correlated with significant functional impairment after wrist trauma, limited research exists on the effects of proprioception and multi sensory training after distal radius fracture.

NCT ID: NCT04907812 Not yet recruiting - Clinical trials for Distal Radius Fracture

The Role of Tranexamic Acid in Reducing Post Operative Hand Edema After Hand and Wrist Surgery

THAW
Start date: June 1, 2021
Phase: Phase 4
Study type: Interventional

Hand edema following hand surgery is a common yet devastating side effect that can lead to early stiffness, prolonged rehabilitation and diminished function. These factors can reduce a patient's quality of life; mounting to an overall delay in recovery, return to work and daily activities. Conventional edema therapy includes cryotherapy, external compression, active and passive exercises and various types of massage. However, there is little evidence to suggest these modalities are effective. Tranexamic acid (TXA) is an antifibrinolytic that has been used in surgical disciplines for decades to aid in reducing intraoperative blood loss and consequent transfusions. Recently, the use of TXA for curbing post-operative edema and ecchymosis has shown promising results, however, its use in hand surgery has not been studied.

NCT ID: NCT04895891 Recruiting - Hand Injuries Clinical Trials

3D Personalized Modelization of the Hand Using EOS Imaging System

M3DME
Start date: October 6, 2020
Phase: N/A
Study type: Interventional

This study aims to compare the quality of 3D hand modelization with EOS imaging with gold-standard computed tomography

NCT ID: NCT04832490 Completed - Clinical trials for Wounds and Injuries, Feet

ULD-E (Ultra Low Dose Extremities)

ULD E
Start date: February 1, 2018
Phase:
Study type: Observational

extremity trauma is a frequent reason for emergency room visits. There is an increase in the use of CT scanners in extremity trauma, due to a greater sensitivity of detection than X-rays, particularly for "occult fractures" and for the organization of treatment, particularly surgical treatment. As the number of CT scans increases, the reduction of the delivered dose has become a subject of interest. Among the many methods used, the use of iterative reconstruction has enabled a substantial reduction in the delivered dose without compromising image quality: low-dose and ultra-low-dose protocols (effective dose equivalent to the effective dose of the Diagnostic Reference Levels of radiographs from the same region of interest) have been developped, but have not yet been evaluated in extremity trauma. The subject of our feasibility study is to evaluate the diagnostic performance of ultra-low dose CT compared to radiographs in patients consulting for extremity trauma in the emergency room. The recent implementation in our department of a scanner dedicated to low-dose explorations as well as the optimization of protocols has allowed the realization of ultra-low-dose scans since June 2017.

NCT ID: NCT04802564 Recruiting - Hand Injuries Clinical Trials

Musical Biofeedback for Sensorimotor Control Capacity of Hands

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

In the proposed study, the investigators assumed that music support treatment, a multisensory-based framework for ameliorating brain plasticity, combined with low-amplitude vibration stimulation can prime motor system and change in motor performance for the patient with a peripheral injury or the loss of a limb. The specific aim of this study is to develop a Multisensory Biofeedback with Musical Interface system, with the aim of improving the sensorimotor impairment of patients' hands.The expected outcomes of this research are to clarify the effects of application Multisensory Biofeedback with Musical Interface on motor and hand function for patients with hand injuries.

NCT ID: NCT04780906 Completed - Sport Injury Clinical Trials

Influence of Wrist Taping on Handgrip Strength in Crossfit Athletes

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The idea that the use of a wristband can increase the grip strength is old, but without systematic scientific evidence. Most Crossfit practitioners wear wrist bands during training because it is believed that the wristband increases the grip strength of the hand. The aim of this study is to to analyze the influence of the use of the wristband on the maximum force value and on the dynamic resistance of hand hold. A simple blind randomized cross-over trial will be performed.

NCT ID: NCT04728607 Active, not recruiting - Wounds and Injuries Clinical Trials

Use of a Compression Device for Ring Removal: A Prospective Trial

Start date: July 26, 2021
Phase: N/A
Study type: Interventional

The usual treatment for stuck rings includes a variety of techniques including use of ice to reduce swelling, use of lubricants, and sometimes the use of string or ring cutters. The success rate of these techniques is variable and cutting the ring is usually reserved as a last resort. Sometimes removal of a ring can take time, and can cause some small injury to the patient. Because of this, it is important to consider other methods for ring removal. This study is looking at using a device that uses compression to reduce swelling of the finger causing the ring to be stuck. This device has been approved for use in Canada. The purpose of this study is to evaluate how effective a compression device is at removing stuck rings. The study question is: how effective is a compression device at removing stuck rings? A Compression Device (CD) is a device that uses circumferential compression to reduce swelling around a stuck ring. The device is used by placing it near, but not over-top, the offending ring, and then is inflated compressing the finger. The device is applied, and the hand elevated, for approximately five minutes. The device is then removed, and with a small amount of lubricant, the ring is removed. All patients requiring ring removal at the QEII emergency department, if a compression device can be used safely, will be asked if they would like to be included in the study and have their ring removal attempted by a compression device. Following removal attempt, the clinician will document information about the ring removal. This will include some questions regarding the patient's experience with the removal. No identifying information or personal health information will be recorded. The investigators plan to collect information about use of the compression device for a period of one year. Following this time, the data will be analyzed to determine how effective the compression device is at removing rings including statements regarding patient experience. This information will be documented in a manuscript intended for publication and may be presented at academic conferences or other continuing education events. The investigators will be measuring the success rate of ring removal with the compression device. In addition, the investigators will record information on any side effects of use of the compression device, as well as patient experience including pain and satisfaction.

NCT ID: NCT04673877 Completed - Infection Clinical Trials

Vancomycin Tissue Concentrations by Bier Block or Intravenous Administration

Start date: August 26, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether or not giving a lower dose of antibiotics (Vancomycin) in the area where it is needed (upper extremity) is more effective at preventing infection than the current standard dose which is given intravenously (IV).

NCT ID: NCT04646343 Recruiting - Clinical trials for Hand Injuries and Disorders

Cross-cultural Adaptation and Validation of the CISS and the PWES Questionnaire in Patients With Hand Pathologies.

Start date: December 1, 2020
Phase:
Study type: Observational

The primary objective of the study is to do translation, cross-cultural adaptation and validation of the CISS and PWES questionnaire in French. No available translation exist in French. In the first part of the study, the investigators will use clinical guidelines for translation and cross-cultural adaptation of questionnaire (Beaton and al).The content validity will be evaluated also in this first step. In the second part of the study the French version of CISS and PWES (F-CISS and F-PWES) will be validated. Different psychometric properties (internal consistency, test retest reliability, construct validity, floor and ceiling effects) will be study. The investigators use the recommendation of COSMIN (COnsensus- based Standards for the selection of health Measurement INstruments) group.

NCT ID: NCT04625868 Completed - Surgery Clinical Trials

Effectiveness of a Preoperative Educational Video for Reducing Opioid Consumption After Hand Surgery

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

This study seeks to determine if watching a preoperative educational video influences opioid consumption and proper disposal following elective hand surgery.