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Chest Trauma clinical trials

View clinical trials related to Chest Trauma.

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NCT ID: NCT05342103 Completed - Chest Trauma Clinical Trials

High Flow Nasal Oxygenation Versus Non-invasive Ventilation for Patients With Blunt Chest Trauma

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Chest trauma remains an issue for health services for both severe and apparently mild trauma management. Severe chest trauma is associated with high mortality and is liable for 25% of mortality in multiple traumas. Moreover, mild trauma is also associated with significant morbidity, especially in patients with preexisting conditions. Thus, whatever the severity, a fast-acting strategy must be organized. In order to improve the prognosis of patients with severe chest trauma, early and continuous application of non-invasive mechanical ventilation (NIV) can indeed reduce the need for intubation and shorten intensive care unit length-of-stay. Among different mechanisms, the early use of positive end-expiratory pressure after chest trauma, when feasible, seems mandatory to optimize oxygenation and improve clinical outcomes. Indeed, interventions aimed at preventing ARDS after chest trauma carry the greatest potential to reduce the substantial morbidity, mortality, and resource utilization associated with this syndrome.

NCT ID: NCT05175781 Completed - Chest Trauma Clinical Trials

Sedation for Non-invasive Ventilation in Blunt Chest Trauma

Start date: January 18, 2022
Phase: N/A
Study type: Interventional

Effectiveness of sedation using dexmedetomidine and ketamine to facilitate non-invasive ventilation sessions which improve overall outcome after blunt chest trauma

NCT ID: NCT04748003 Completed - Chest Trauma Clinical Trials

Acute Myocardial Dysfunction and Chest Trauma - The Strainy Trauma Study

Strainy trauma
Start date: February 28, 2021
Phase:
Study type: Observational

This study aims to investigate whether the identification of acute myocardial dysfunction by 2D-strain transthoracic sonography in the first week following trauma would allow to better diagnose occult and severe patterns of myocardial contusion, in order to identify a subpopulation at higher risk of complications. The measurement of myocardial strain (2D-strain) by transthoracic sonography is a robust tool to assess the myocardial function. The investigators strongly suppose that the 2D-strain would allow to better identify subclinical MC in chest trauma, as well as the severe patterns that are associated with more organs dysfunctions and a worst outcome.

NCT ID: NCT04318496 Completed - Rib Fractures Clinical Trials

Acupuncture for Blunt Chest Trauma

Start date: March 23, 2020
Phase: N/A
Study type: Interventional

Introduction: Chest blunt trauma accounts in up to 65% of polytrauma patients. In patients with 0-2 rib fracture, the treatment is relatively limited to oral pain killer and breathing exercise. The patients will suffer two weeks of severe pain accompanied with poor sleep and inability to preform simple daily live activities. In this double blind randomized control study, the investigators offer acupuncture as an additional treatment option. Methods: The study is a double blind randomized control trial. the study will include the press needle acupuncture (Acu) and placebo (Con) group. Both groups will receive one treatment, following the first visit to the clinic after chest trauma accident.

NCT ID: NCT03797079 Completed - Chest Trauma Clinical Trials

Erector Spinae Plane Block Versus Thoracic Epidural Block for Chest Trauma

Start date: January 20, 2019
Phase: N/A
Study type: Interventional

Rib fractures are very common as a consequence of blunt chest trauma which is associated with severe pain, morbidity and mortality. The key to managing these patients is prompt and effective analgesia, early mobilization, respiratory support, with chest physiotherapy. The aim of this study is to compare and evaluate the differences between either continuous erector spinae plane (ESP) block, or thoracic epidural analgesia (TEA) as analgesic modalities in patients with chest trauma. It is hypothesized that ESP block will be comparable to TEA as a promising effective analgesic alternative with fewer side effects.

NCT ID: NCT01134744 Completed - Chest Trauma Clinical Trials

Evaluating Validity of Clinical Criteria for Requesting Chest X-Rays in Trauma Patients

Start date: October 2006
Phase: N/A
Study type: Observational

The purpose of this study is to identify the clinical criteria for requesting a chest x-ray in a patient with blunt trauma and its findings such as clinical signs with a high sensitivity could be used in a larger study to codify the final criteria.