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Contusions clinical trials

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NCT ID: NCT06386120 Not yet recruiting - Lung Contusion Clinical Trials

Respiratory Function Monitoring of Mechanical Ventilation in Patients With Chest Blunt Injury

Start date: May 2024
Phase:
Study type: Observational

The goal of this observational study is to learn about EIT in observing the application of lung protective ventilation strategies in patients with pulmonary contusion, particularly the impact on pulmonary ventilation blood flow ratio, oxygen, and condition. The main question it aims to answer is: Can lung protective ventilation strategies improve respiratory function in patients with severe chest contusion? We will collect clinical data of participants who already taking lung protective ventilation strategies as part of their regular medical care.

NCT ID: NCT06065046 Not yet recruiting - Clinical trials for Traumatic Brain Injury

Baricitinib for Moderate and Severe Traumatic Intracerebral Hemorrhage/Contusions

Start date: October 2023
Phase: Phase 2
Study type: Interventional

The purpose of the present study is to study the effect of baricitinib administration on outcome of participants with moderate and severe traumatic intracerebral hemorrhage/contusions. A multi-center randomized control trial will be conducted. Participants with a radiological diagnosis of traumatic intracerebral hemorrhage/contusions and an initial GCS score of 5-12 will be screened and enrolled in the first 24 hours after traumatic brain injury.

NCT ID: NCT05156008 Not yet recruiting - Clinical trials for Vascular Access Complication

Comparison of Ultrasound-guided and Palpation-inserted Peripheral Venous Cannula

CompOne
Start date: July 1, 2023
Phase: N/A
Study type: Interventional

Every patient need venous access for surgery under anesthesia. It is the most frequently performed invasive procedure in medicine in the whole world. In expert groups, ultrasonographically guided vascular access (UGVA) appears to be a significantly better method, but studies on larger groups of patients are lacking. Prospective randomized 2-arm study which is comparing success rate of ultrasound guided a palpation inserted cannulas in patients undergoing primary hip or knee arthroplasty. The project will be managed according to the protocol of principles of Good Clinical Practice and valid regulations.

NCT ID: NCT05109000 Not yet recruiting - Anesthesia, Local Clinical Trials

Comparison of Subcutaneous Injection of Normal Saline and Bacteriostatic Saline

Start date: November 2021
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blind, single-center clinical trial comparing normal saline and bacteriostatic saline subcutaneous injection within a single subject. While both normal saline and bacteriostatic saline can be administered intravenously, this study aims to investigate their effects following subcutaneous injection. While benzyl alcohol (the bacteriostatic component of bacteriostatic saline) is known to have local anesthetic properties, it also is an irritant and can cause inflammation at the injection site. Based on clinical experience investigators anticipate that a normal saline injection will cause a mild stinging sensation and no subsequent inflammation. In contrast, subcutaneous injection of bacteriostatic saline will not cause stinging but will cause a mild degree of inflammation which is manifested as mild tenderness and mild ecchymosis at the site of injection.

NCT ID: NCT05054270 Not yet recruiting - Lung Injury Clinical Trials

Efficacy of Lung Ultrasound in Monitoring Fluid Resuscitation in Chest Trauma Patients

Start date: September 30, 2021
Phase:
Study type: Observational

Efficacy of Lung ultrasound in monitoring fluid resuscitation in chest trauma patients with lung contusions

NCT ID: NCT04533269 Not yet recruiting - Bruise, Contusion Clinical Trials

A Study of Topical Arnica & Ledum on Bruise Reduction in HNV

Start date: July 31, 2021
Phase: N/A
Study type: Interventional

Subjects will have a bruise induced. A pad containing either a placebo or active will be applied to the bruise. Photographs will be taken over the following days to record bruise healing.

NCT ID: NCT01097798 Not yet recruiting - Trauma Clinical Trials

To Evaluate the Efficacy and Safety Aliviador Compared to Gelol in Patients With Contusions, Sprains, Trauma and Muscle Injury.

LBB-ALI-01/09
Start date: June 2010
Phase: Phase 3
Study type: Interventional

Multicenter, randomized, double-blind trial, to evaluate the efficacy and safety Aliviador compared to Gelol in the relief of signs and symptoms in patients with contusions, sprains, trauma and muscle injury start with less than 24 hours or patients of myalgia, myofascial pain and tendinitis.

NCT ID: NCT00970658 Not yet recruiting - Pain Clinical Trials

Efficacy and Safety of Salonsip Compared to Sabiá Plaster

SAL-SIP-03/09
Start date: December 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy in reducing signs and symptoms in patients with contusions, sprains, muscular injuries and injuries with less than 24 hours early or holders of myalgia, pain and tendonitis in regions miofasciais articulated with Salonsip compared to Sabiá plaster. It is clinical, open, multicenter, randomized, prospective and comparative, with patients entering at random. Patients will be included in sufficient quantity to achieve the minimum number of 70 evaluable patients.