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Polytrauma clinical trials

View clinical trials related to Polytrauma.

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NCT ID: NCT05221476 Completed - Clinical trials for Comorbidities and Coexisting Conditions

Red Blood Cell Distribution Width and Charlson Comorbidity Indeces in the Frail Polytraumatized Patient.

Start date: January 2012
Phase:
Study type: Observational

In this study patients who were admitted to our hospital with critical injuries were enrolled retrospectively from January 2012 to December 2015. Patients with an ISS>16 points, an AIS >3 in one body region and at least 2 different body regions affected were included. RDW values on admission as well as preexisting comorbidities were evaluated.

NCT ID: NCT05074095 Completed - Polytrauma Clinical Trials

Analysis of Urogenital Injuries in Polytraumatized Patients

Start date: January 1, 2016
Phase:
Study type: Observational

Urogenital injuries occur in approximately 5-10 % of all severly injured patients. The literature lacks a thorough investigation into the mechanisms of trauma, the analysis of the whole urogenital tract and especially the correlation of thoracic and lumbar spine and pelvic injuries with urogenital injuries. The goal of this study is to provide a thorough investigation into these primary end points in a multicenter study of university hospitals in Germany.

NCT ID: NCT04766944 Not yet recruiting - Critical Illness Clinical Trials

Incidence and Associated Risk Factors of ARC in the Trauma Critically Ill Older Than 50 Years Old

Start date: March 2024
Phase:
Study type: Observational

This single-center prospective cohort study conducted at the adult trauma ICU of the Montreal General Hospital (MGH) affiliated with the McGill University Health Centre (MUHC) aims to determine the incidence and associated risk factors of augmented renal clearance (ARC) in critically ill trauma patients of 50 years old and above.

NCT ID: NCT04723992 Completed - Polytrauma Clinical Trials

25-Year Experience With Polytraumatized Patients in a Level 1 Trauma Center

Start date: January 1992
Phase:
Study type: Observational

In this study patients who were admitted to our hospital with critical injuries were enrolled retrospectively from January 1992 to December 2019. Patients with an ISS>16 points, an AIS >3 in one body region and at least 2 different body regions affected were included. Possible prognostic factors were evaluated.

NCT ID: NCT04683094 Completed - Sepsis Clinical Trials

Comparative Study for the Validity of Various Severity Scoring System

Start date: April 1, 2020
Phase:
Study type: Observational

Scoring systems for use in intensive care unit (ICU) patients have been introduced and developed over the last 30 years. They allow an assessment of the severity of disease and provide an estimate of in-hospital mortality

NCT ID: NCT04410952 Completed - Polytrauma Clinical Trials

Pelvic Binder vs. Pelvic C-clamp for Bleeding Control

Start date: January 7, 2020
Phase:
Study type: Observational

Pelvic ring fractures carry a high risk for severe bleeding. Expecially bleeding from the posterior ring might result in a fatal course. Different types of external emergency stabilization (EES) are available for the posterior pelvic ring, namely the non-invasive pelvic binder or the invasive pelvic c-clamp. Which stabilization technique is superior, has not been investigated yet.

NCT ID: NCT04335838 Completed - Clinical trials for Traumatic Brain Injury

Age, Traumatic Brain Injury and Injury Severity as Independent Risk Factors for In-Hospital Mortality in Polytrauma Patients.

Start date: January 2012
Phase:
Study type: Observational

In this study patients who were admitted to our hospital with critical injuries were enrolled retrospectively from January 2012 to December 2015. Patients with an ISS>16 points, an AIS >3 in one body region and at least 2 different body regions affected were included. Possible prognostic factors were evaluated.

NCT ID: NCT04107818 Completed - Clinical trials for Coagulation Disorder

Comparison of Viscoelastic Measurement by ROTEM® Delta and ClotPro® in Trauma Patients.

ROTCLOT
Start date: November 21, 2019
Phase:
Study type: Observational

The purpose of the study is to describe the differences and interchangeability in measurements of viscoelastic tests of coagulation by two different devices in adult trauma patients.

NCT ID: NCT03952026 Completed - Polytrauma Clinical Trials

Impact of Associated Abdominal Injuries on Clinical and Operative Outcome in Pelvic Injuries

Start date: December 6, 2018
Phase:
Study type: Observational [Patient Registry]

Pelvic fractures are severe injuries which require advanced orthopedic surgical skills to treat. On the other hand, abdominal injuries are severe injuries, which might require quick general surgical treatment. The combination of both injuries is a challenge for orthopedic surgeons, as the abdominal injury might lead to a delayed surgical treatment of the pelvic fracture. Whether an associated abdominal injury influences the quality of care of pelvic fractures, is aim of this registry study.

NCT ID: NCT03906721 Completed - Clinical trials for Spinal Cord Injuries

Reduction of Opioid Dose Using Conditioning & Open-Label Placebo (COLP) in Patients With Spinal Cord Injury, Polytrauma and Burn Injury

Start date: February 20, 2019
Phase: Phase 2
Study type: Interventional

The use of conditioning open-label placebo (COLP) will be studied as a dose extension method to lower opioid dosage in patients with spinal cord injury, polytrauma, and burn injury. The goal is to provide the same level of pain relief with a reduced opioid dose to diminish adverse effects as well as the risk of addiction associated with narcotic treatment.