Registry for traumatic vascular injuries
Registry for Vascular Trauma and Follow-up Examinations
This study is creating a database to track patients with vascular injuries from trauma to see how different treatments affect their recovery and improve care for future patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital Augsburg Academic / other |
| Locations | 1 site (Augsburg) |
| Trial ID | NCT05846321 on ClinicalTrials.gov |
What this trial studies
This project establishes a registry at Augsburg University Hospital for patients with isolated vascular trauma or vascular involvement in poly-trauma. The aim is to collect data on therapeutic procedures and outcomes for this rare complication of trauma. By pooling data, the study seeks to understand the long-term outcomes of patients who typically do not have pre-existing vascular diseases, as their physiological responses differ from those with vascular conditions. This registry will help improve treatment protocols and patient care for vascular injuries.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who have experienced vascular involvement in trauma.
Not a fit: Patients who are minors or unable to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance understanding and treatment of vascular trauma, leading to improved patient outcomes.
How similar studies have performed: While this approach is focused on a specific registry for vascular trauma, similar registries have shown success in improving outcomes in other trauma-related studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age over 18 years * Vascular involvement in trauma * Isolated vascular injury * Written informed consent, except for those deceased from trauma sequelae Exclusion Criteria: * Minority * Lack of consent
Where this trial is running
Augsburg
- University Hospital Augsburg — Augsburg, Germany (Recruiting)
Study contacts
- Study coordinator: Yvonne Gosslau, MD
- Email: yvonne.gosslau@uk-augsburg.de
- Phone: +49 821/4002655
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.