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Neck Injuries clinical trials

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NCT ID: NCT05576857 Recruiting - Clinical trials for Hyperextension Injury of Neck

Effects of Cervical Hyperextension on Cervical Blood Flow, Cerebral Oximetry and Cognitive Functions.

Start date: March 29, 2021
Phase:
Study type: Observational

The goal of this observational study is to determine the effects of cervical hyperextension on cerebral oximetry and cognitive functions in healthy individuals without other additional factors such as anesthesia and surgical stress. The main questions it aims to answer are: - Can cervical hyperextension cause changes in cerebral oxygenation in non-anesthetized healthy individuals? - Can cervical hyperextension cause changes in cervical and cerebral blood flow in non-anesthetized healthy individuals? - Can cervical hyperextension cause changes in cognitive functions in non-anesthetized healthy individuals? - Can cervical hyperextension cause changes in optic nerve sheath diameter in non-anesthetized healthy individuals? Participants will be monitored with cerebral oximeter device and asked to answer Montreal cognitive function test before and during cervical hyperextension position. The researchers will evaluate the changes in cervical and cerebral blood flow ultrasonographically before and during cervical hyperextension position.

NCT ID: NCT04615338 Recruiting - Neck Injuries Clinical Trials

Outcomes and Trauma Pattern in Penetrating Neck Injuries

Start date: October 1, 2020
Phase:
Study type: Observational [Patient Registry]

It is an observational retrospective multicenter study

NCT ID: NCT04066686 Completed - Neck Injuries Clinical Trials

Evaluation of Comfort in a Spinal Collar

Start date: October 26, 2018
Phase:
Study type: Observational

This is an observational study which aims to assess the comfort of a spinal collar in patients who have them fitted as part of their clinical care due to neck injury.

NCT ID: NCT03949959 Completed - Whiplash Injuries Clinical Trials

Effectiveness of Physiotherapy Following PRP for Chronic Whiplash

Start date: March 4, 2019
Phase: N/A
Study type: Interventional

The investigators will explore a standardized and previously published evidence-based conservative multimodal physiotherapy treatment fulfilling clinical practice guidelines in individuals with chronic whiplash-associated disorders (WAD) with facet-mediated pain (appropriate response to dual medial branch blocks) undergoing cervical facet joint Plasma-Rich Platelet (PRPt) and compare health outcomes to individuals' undergoing cervical facet joint PRP with usual care (PRPu), which consists of advice, supervised home exercise and pharmacological management for treatment of residual pain. To be clear, the investigators are not investigating the efficacy or effectiveness of cervical facet joint PRP - these individuals have already consented to proceed with PRP treatment. The investigators are evaluating the role of adjuvant conservative multimodal physiotherapy treatment. It must be noted that these patients have previously failed to respond to conservative physiotherapy. The investigators will use a design which is quite novel in physiotherapy, Single Case Experimental Designs (SCEDs). In contrast to an experimental group design in which one group is compared with another, participants in single-subject research provide their own control data for the purpose of comparison in a within-subject rather than a between-subjects design. SCEDs provide a method to determine response and benefit for every individual patient. Therefore, the investigators will assess effectiveness of conservative multimodal physiotherapy for chronic WAD with facet-mediated pain undergoing cervical facet joint PRP, using patients as their own control, in a multiple baseline design.

NCT ID: NCT03698214 Completed - Clinical trials for Traumatic Brain Injury

Is There a Worse Outcome When the Systolic Blood Pressure is Lower Than Heart Rate in Those Adult Trauma Patients With Isolated Head/Neck Injury

Start date: March 23, 2016
Phase:
Study type: Observational

A systolic blood pressure (SBP) lower than the heart rate (HR) could indicate a poor condition in trauma patients. In such scenarios, the reversed shock index (RSI) is <1, as calculated by the SBP divided by the HR. This study aimed to clarify whether RSI could be used to identify high-risk adult patients with isolated traumatic brain injury (TBI).

NCT ID: NCT03252886 Completed - Clinical trials for Cardiopulmonary Arrest

Videolaryngoscopy During CPR for Trauma Patients

Start date: March 1, 2011
Phase: N/A
Study type: Interventional

This is a clinical study based on collected video-clip data of cardiopulmonary resuscitation for patients with suspected neck injury in multiple trauma between 2011 and 2015. The study aimed to compare all possible factors relating to ETI performance during CPR for truma patients between experienced video-laryngoscopy and direct- laryngoscopy users.

NCT ID: NCT02786966 Completed - Neck Injuries Clinical Trials

A Pragmatic Evaluation of the Canadian C-Spine Rule by Paramedics

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

Each year, half a million patients with a potential neck (c-spine) injury are transported to Ontario emergency departments (ED). Less than 1% of all these patients actually have a neck bone fracture. Even less (0.5%) have a spinal cord injury or nerve damage. These injuries usually occur at the time of initial trauma and not during transport to the ED. Currently, paramedics transport all trauma victims (with or without an injury) by ambulance using a backboard, collar, and head immobilizers. Trauma victims can stay immobilized for hours until an ED bed is made available or until x-rays are completed. Importantly, long immobilization is often unnecessary, it causes patient discomfort and pain, decreases community access to paramedics, contributes to ED crowding, and is very costly. The investigators developed the Canadian C-Spine Rule (CCR) for alert and stable trauma patients. This decision rule helps ED physicians and triage nurses to safely and selectively remove immobilization, without x-rays and missed injury. The investigators will evaluate the possibility and benefits of allowing paramedics to use the CCR in the field in 12 new communities from across Ontario. Patients have suggested the investigators include measures of pain and discomfort from being immobilized during transport as important patient-centred outcomes. The investigators will also measure the impact on the ED, and how much money could be saved if more paramedics were allowed to use the CCR. The investigators will also assess if sex, age, language barriers, or living far from the hospital (long transport time) will affect the outcomes of the study.

NCT ID: NCT00266929 Completed - Spinal Injuries Clinical Trials

Treatment of Type II Odontoid Fractures Among the Elderly

Start date: December 2005
Phase: N/A
Study type: Observational

The purpose of this study is to compare the safety and effectiveness of surgical versus conservative management of type II odontoid fractures among patients > 64 years of age. Of secondary interest is to determine if there are differences in outcomes between anterior screw fixation and posterior fusion of these fractures.

NCT ID: NCT00154622 Completed - Back Injury Clinical Trials

Management and Outcome of Work-Related Musculoskeletal Disorders

Start date: January 2004
Phase: N/A
Study type: Interventional

Work-related musculoskeletal disorders(MSD)are very common,which account for most of the occupational compensation in U.S.A。According to the epidemiological surveys,injured sites are frequent at low back,neck and shoulder and upper extremity。Although the MSD will not threaten the lives,they result in discomfort,some cost much and decrease the productivity。There was little study in our country to reveal the risk factors of medical utilization and disabling of MSD。Therefore,we do not have well-established strategy of the assessment and treatment for the workers who can not return to work。The purposes of this study are:1、To have sequential surveys to find the prevalence,incidence and possible risk factors of work-related MSD of employees in different industries and their medical utilization and disabled conditions。2、To find the victims of work-related MSD from clinics,assess their disablement and if they return to work and to find the factors those prevent them return to work。3、To develop individualized work hardening programs for the victims who can not return to wok after treatment。The program will be established according to their injuries and their work characteristics。