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Flail Chest clinical trials

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NCT ID: NCT04710602 Completed - Clinical trials for Rib; Fracture, Multiple, With Flail Chest

Prospective Follow up of Minimally Invasive Chest Wall Surgery After Trauma

Start date: January 15, 2021
Phase:
Study type: Observational

The purpose of this study is to assess the outcome of a muscle sparing, minimally invasive open surgical technique for unstable ribcage injuries after trauma. The investigators will compare the results from the study participants to a historical cohort who were operated with a different surgical technique with large incisions and simultaneous thoracotomy.

NCT ID: NCT03090308 Completed - Pulmonary Contusion Clinical Trials

Pulmonary Contusion Flail Chest Complex

Start date: April 2013
Phase: N/A
Study type: Observational [Patient Registry]

The study included 20 adult patients presented by multiple fractured ribs (flail segment) with thoracic trauma severity score (TTSS) between 5 and 15. All patients received mid-thoracic epidural analgesia with 0.125% Bupivacaine and 1 μg/ml fentanyl. The patients were ventilated using non-invasive positive pressure ventilation (NIPPV). Follow up arterial blood gases, chest X-ray and CT scan were obtained. Parameters to be recorded: Patient's characteristics and clinical data including pulmonary contusion, number of fractured ribs, pleural involvement, PaO2/FiO2 ratio on admission, weaning outcome, duration of NIPPV, length of stay in ICU (LOS ICU), complications and mortality rate.

NCT ID: NCT02132416 Completed - Surgery Clinical Trials

Operative Treatment of Unstable Thoracic Cage Injuries and Chest Wall Deformity in Trauma

Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of this prospective controlled study is to determine whether surgical management of unstable thoracic cage injuries and chest wall deformity in trauma reduces the need for and the time spent on ventilator compared to a group treated without operation.

NCT ID: NCT01308697 Completed - Flail Chest Clinical Trials

Flail Chest: A Randomized Controlled Study

Start date: April 2011
Phase: N/A
Study type: Interventional

Flail chest refers to a section of the rib cage that has broken away from the surrounding ribs. Usually, more than one rib is involved, and they are broken in at least two places. Flail chest typically is the result of blunt chest trauma. As a result of flail chest, the chest wall becomes unstable and dangers of life threatening respiratory failure and hypoxemia (lack of oxygen to circulating blood which will lead to organ damage or failure)occur. Currently, these injuries are treated non operatively. However, small case series have demonstrated that operative management can improve Intensive Care Unit (ICU) length of stay, improved pulmonary function and decreased pain leading to decreased duration of mechanical ventilation, and the incidence of complications related to this injury. This study hopes to provide information on whether a prospective randomized trial is feasible by first undertaking a small pilot study to determine rate of recruitment, data collection methods, and integrity of study protocol. Null Hypothesis 1: Enrollment of subjects with flail chest rib fractures into a prospective multi-centre RCT is not feasible and a larger clinical trial is unlikely to be completed.

NCT ID: NCT00810251 Completed - Flail Chest Clinical Trials

MatrixRIB Implants for Surgical Stabilization of Flail Chest Injuries: A Registry

MatrixRIB
Start date: December 2008
Phase: Phase 4
Study type: Observational

The purpose of this observational study is to document the treatment of serial rib fractures with MatrixRIB implants in a registry.

NCT ID: NCT00556543 Completed - Rib Fracture Clinical Trials

Clinical Study of the U-Plate Fracture Repair System to Treat Rib Fractures

Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to gather information about a device used to help fix broken ribs. Hypothesis: Rib fracture repair with the U-plate system is clinically durable and safe for the indications of flail chest repair, acute pain control, chest wall defect repair, and rib fracture non-union.

NCT ID: NCT00298259 Completed - Ventilation Clinical Trials

Trial of Operative Fixation of Fractured Ribs in Patients With Flail Chest

Start date: January 2007
Phase: Phase 2
Study type: Interventional

Background: Fracture of several ribs in more than one place as the result of trauma, leads to paradoxical movement of the chest wall and ventilatory failure. The mainstay of management in these patients has traditionally been analgesia and positive pressure ventilation to splint the chest wall and allow healing of the ribs to begin. However, this management option leads to prolonged intensive care unit (ICU) stay with increasing complication rates as patients remain on a ventilator for prolonged periods. Patients often remain on a ventilator for two to three weeks while waiting for enough rib healing to provide sufficient chest wall stability to allow the patient to take over all their breathing themselves. Until that time, patients are at risk of pneumonia and sepsis and other complications. Long term disabilities which have been reported in these patients include ongoing pain syndromes, inability to return to work, particularly manual type labour and cosmetic chest wall deformities. An alternative treatment strategy is to operatively fix the ribs. By fixing the ribs operatively, the patient no longer requires internal pneumatic stabilization (provided by mechanical ventilation) and can be weaned from the ventilator within days rather than weeks. This can potentially lead to earlier discharge from the intensive care unit, and an avoidance of the multiple complications which arise in the ventilated patient. Rib fixation may also lead to less pain and deformity, improved mobility in the post injury phase and earlier return to work. Hypothesis: that early operative fixation of ribs in patients presenting with flail chest secondary to trauma will result in less mechanical ventilatory requirements, earlier discharge from the intensive care unit and lower rate of complications associated with prolonged mechanical ventilation. This will lead to cost savings in the treatment of these patients.