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Rib Fractures clinical trials

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NCT ID: NCT02487264 Completed - Trauma Clinical Trials

Analysis of the Status, Treatment and Outcomes of Rib Fractures

Start date: June 2013
Phase:
Study type: Observational

A retrospective analysis of all patient presenting with multiple rib fractures to the emergency room of Penn State Hershey Medical Center between 2010-2012. Patient demographics, cause of fracture, outcomes, chronic medical conditions, vital signs, length of stay, pain levels and treatment, and sequelae will be recorded and analyzed.

NCT ID: NCT02432456 Completed - Wounds and Injuries Clinical Trials

Ketamine Infusion Therapy for the Management of Acute Pain in Adult Rib Fracture Patients

Start date: September 2015
Phase: Phase 4
Study type: Interventional

This study will evaluate the effectiveness of ketamine infusions in the management of acute pain resulting from broken ribs suffered following a blunt trauma. Half of patients will receive the institutional standard of care and a placebo infusion (no active medication). The other half of patients will receive the institutional standard of care and a ketamine infusion. All subjects and staff will be blinded as to whether they are receiving placebo or ketamine.

NCT ID: NCT02295098 Completed - Wounds and Injuries Clinical Trials

Comparison of Epidural and Paracostal Catheter Placement for Pain Control After Rib Fractures

Start date: August 19, 2015
Phase: N/A
Study type: Interventional

The investigators plan to compare the incidence of successful placement of epidural pain catheters versus paracostal catheters for the control of pain and prevention of pulmonary complications for adult trauma patients with blunt chest wall trauma resulting in multiple rib fractures. When a trauma patient has > or = to 3 rib fractures on the same side, is being admitted to the Surgical ICU, and is encountered within 72 hours from the time of their injury, they will be eligible for the study. If they (or a proxy) choose to participate, consent will be obtained and they will randomly be assigned to receive either an epidural or paracostal catheter for pain control. The aim of the study is to determine if paracostal catheters are noninferior to epidurals for controlling pain in multisystem trauma patients. Secondarily the investigators will evaluate success and time of placement of the assigned intervention and follow the patient throughout their hospital course to compare the success of analgesia provided by each modality along with any complications and/or benefits of the two types of catheters.

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: NCT02028611 Completed - Rib Fracture Clinical Trials

Comparison of Gray-scale Inverted Rib Series With Conventional Ones in Rib Fracture Detection by Emergency Physicians and Medical Students

Start date: June 2013
Phase: N/A
Study type: Observational

There were many studies which examined the availability of inverted gray-scale chest X-ray for increasing the detection of lung nodules. In emergency medicine, rib fracture is an important part for patient's disposition, so investigators designed this study to evaluate the availability of inverted gray-scale chest X-ray for the detection of rib fracture.

NCT ID: NCT01599403 Completed - Clinical trials for Traumatic Rib Fracture

Thoracic Blocks Versus Thoracic Epidural and Patient Controlled Anesthesia in Traumatic Rib Fracture Patients

Start date: April 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to investigate whether continuous PVB is equal in efficacy to epidural anesthesia in terms of analgesia in patients with INR lower than 1.2, or is continuous ICNB equal in efficacy to PCA in terms of analgesia, if patients have INRs equal to or greater than 1.2.

NCT ID: NCT00926991 Completed - Rib Fractures Clinical Trials

Chest Wall Repair of Rib Fractures After Trauma

Start date: August 2009
Phase: N/A
Study type: Observational

This is a prospective, observational trial of 50 patients who have multiple, severe rib fractures following trauma. The investigators will follow their hospital stay for outcomes (infections, length of stay and medical care) as well as their early post-hospital course.

NCT ID: NCT00774618 Completed - Rib Fracture Clinical Trials

Evaluation of Surgical Treatment on Pain and Disability for Chronic, Non-healing Rib Fracture

Start date: October 2008
Phase: Phase 4
Study type: Interventional

Individuals with non-healing rib fractures may experience significant pain and disability. This is called rib fracture non-union, an unusual problem and one that most physicians have little experience with. The investigators hypothesize that surgical repair of rib fracture non-union is clinically efficacious and safe in 6 month follow-up. The objective of this study is to evaluate how repairing non-healing rib fractures affects pain and disability.

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.