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Active Not RecruitingNCT07482267

Evaluation of Patients Suffering From Polytrauma Admitted to the ICU

Evaluation of Patients Suffering From Polytrauma Admitted to the ICU: a Retrospective Cohort Study.

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
417 (estimated)
Sponsor
Jessa Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to assess the number of polytrauma patients admitted to the Intensive Care Unit. In addition, we aim to describe their clinical characteristics, therapeutic management, and clinical outcomes.

Detailed description

Trauma constitutes a major contributor to global mortality and long-term physical disability. The principal causes of traumatic injury include road traffic accidents, falls, drowning, burns, poisoning, interpersonal violence, and acts of war. Collectively, these causes account for approximately 9% of global deaths. Within the broader population of trauma patients, polytrauma patients represent a distinct and clinically significant subgroup, accounting for approximately 25% of trauma-related hospital admissions. Polytrauma is not merely defined as the coexistence of multiple injuries, but rather as a complex clinical condition characterized by a high risk of complications and progressive physiological deterioration. In the early post-traumatic phase, patients may develop severe hemorrhage, hemorrhagic shock, respiratory compromise, or traumatic brain injury. In the subsequent phase, systemic inflammatory response syndrome, sepsis, and multiple organ dysfunction syndrome may occur. Advances in injury prevention strategies and improvements in trauma care have led to increased survival during the early stages following injury. As a result, a growing number of polytrauma patients require admission to the Intensive Care Unit (ICU), underscoring the need to optimize critical care delivery in this population. The provision of high-quality, evidence-based care depends on the systematic collection and analysis of comprehensive clinical data to facilitate continuous improvement in treatment strategies and outcomes.

Conditions

Timeline

Start date
2025-04-10
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2026-03-19
Last updated
2026-03-19

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT07482267. Inclusion in this directory is not an endorsement.