Analyzing activities during aortic aneurysm ruptures
Analysis of Individual Activity at the Time of Aortic Rupture in Patients With Abdominal Aortic Aneurysms
University Hospital Augsburg · NCT06365138
This study looks at what people were doing when their aortic aneurysm ruptured to see if certain activities or stress levels can help guide safer behaviors for others with similar conditions.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital Augsburg (other) |
| Locations | 1 site (Augsburg) |
| Trial ID | NCT06365138 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the activities patients were engaged in at the time of aortic rupture due to abdominal aortic aneurysms. It will analyze factors such as physical and emotional stress that may contribute to the risk of rupture. By examining these activities, the study seeks to provide insights that could inform guidelines for patients with intact aneurysms regarding safe behaviors. The research will be conducted at the University Hospital Augsburg, focusing on patients who have experienced a rupture.
Who should consider this trial
Good fit: Ideal candidates include patients who have experienced a ruptured abdominal aortic aneurysm and can provide consent.
Not a fit: Patients without a history of aortic aneurysm rupture or those unable to provide consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved guidelines for patients with aortic aneurysms, enhancing their quality of life and safety.
How similar studies have performed: While there is limited research specifically on activities at the time of aortic rupture, related studies on aortic dissections suggest that emotional stress may play a role, indicating potential for novel insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * inclusion of all patients with ruptured aortic aneurysm in Augsburg University Hospital * Written consent to participate in the study by the patient or their legal representative Exclusion Criteria: * Lack of consent
Where this trial is running
Augsburg
- University Hospital Augsburg — Augsburg, Germany (RECRUITING)
Study contacts
- Study coordinator: Tobias Warm, MD
- Email: tobias.warm@uk-augsburg.de
- Phone: +49821400161068
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.
Conditions: Aortic Aneurysm, Aortic Rupture, Physical stress, Emotional Stress, Rupture Risc, Follow-Up, Activity