Understanding how patient body shape affects surgery on the abdominal aorta
Study of the Size of the Operating Fields Depending on the Morphology of the Patients
This study looks at how a person's body shape affects the surgery on the abdominal aorta to help doctors plan better and improve outcomes for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Geprovas Research network |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT06063395 on ClinicalTrials.gov |
What this trial studies
This observational study aims to analyze the relationship between patient morphology and the size of the operating field during open abdominal aorta surgery. By utilizing preoperative CT scans and measuring the working volume during surgery, researchers will develop a mathematical model to predict surgical risks based on individual patient characteristics. The study will include adult patients undergoing this specific surgical procedure and will gather data to enhance surgical planning and outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who are scheduled for open surgery on the abdominal aorta and have undergone a preoperative CT scan.
Not a fit: Patients requiring emergency surgery or those without a preoperative CT scan may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced risks for patients undergoing abdominal aorta surgery.
How similar studies have performed: While this approach is innovative, similar studies have not been widely reported, indicating a novel exploration in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients over 18 years of age * Patient undergoing open surgery on the abdominal aorta by laparotomy. * Patient who has been informed of the terms of the study and who has not expressed non-opposition. Exclusion Criteria: * Emergency surgery * Patient without preoperative CT scan
Where this trial is running
Strasbourg
- Hôpitaux Universitaires de Strasbourg — Strasbourg, France (Recruiting)
Study contacts
- Principal investigator: Nabil Chakfe — Hôpitaux Universitaires de Strasbourg
- Study coordinator: Maxime BEUTELSTETTER
- Email: maxime.beutelstetter@gepromed.com
- Phone: 0671657194
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.