Examining hormone levels in trauma patients
A Prospective Analysis of the Gender Specific Role of Steroid Hormones on the Outcome on Patients After Polytrauma
This study is trying to see how hormone levels in people who have had severe trauma affect their recovery and survival.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Technical University of Munich Academic / other |
| Locations | 1 site (München, Bavaria) |
| Trial ID | NCT05794256 on ClinicalTrials.gov |
What this trial studies
This observational study aims to establish a registry to investigate the role of steroid hormones in patients who have experienced severe trauma. It will measure hormone levels upon arrival at the emergency room and during the following days, while also collecting detailed health-related information through questionnaires. The primary focus is to determine how these hormone levels may influence morbidity and mortality in severely injured individuals.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 who have experienced polytrauma with an Injury Severity Score of 16 or higher.
Not a fit: Patients who are pregnant, deceased upon arrival, incarcerated, or transferred from another facility may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into how hormone levels affect recovery and outcomes in trauma patients.
How similar studies have performed: While the specific approach of this study may be novel, similar studies investigating hormone levels in trauma patients have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Polytrauma with ISS≥16, * severe traumatic brain injury (AIS ≥3) * over the age of 18 * must reach emergency room alive Exclusion Criteria: * pregnant patients * dead on arrival to the hospital * incarcerated patients * secondarily transferred patients
Where this trial is running
München, Bavaria
- Technical University Munich — München, Bavaria, Germany (Recruiting)
Study contacts
- Study coordinator: Olivia Mair, MD
- Email: oliviaanna.mair@mri.tum.de
- Phone: +498941409382
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.