Observational study on patients undergoing endovascular treatment for vascular conditions
OUTCOME IN NEURORADIOLOGIA INTERVENTISTICA INDICAZIONI COMPLICANZE (ONIRIC)
This study looks at patients of all ages getting endovascular treatment for brain or spine blood vessel issues to see how they do before and after the procedure and to find out what might affect their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Sex | All |
| Sponsor | Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta Academic / other |
| Locations | 1 site (Milan) |
| Trial ID | NCT06805721 on ClinicalTrials.gov |
What this trial studies
This three-year observational study involves patients of all ages who are undergoing endovascular treatment for various cerebral or spinal vascular conditions, such as aneurysms and arteriovenous malformations. The study aims to assess both pre- and post-operative clinical conditions, report any complications, and identify preoperative indicators that may predict treatment outcomes. Participants will also receive psychological support and undergo neuropsychological assessments, with clinical, medical, and demographic data collected during hospitalization and follow-up visits.
Who should consider this trial
Good fit: Ideal candidates include patients of any age and sex who are referred for interventional endovascular procedures for cerebral or spinal vascular pathologies.
Not a fit: Patients who are not candidates for interventional endovascular procedures will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve understanding of treatment outcomes and enhance patient care for those undergoing endovascular procedures.
How similar studies have performed: While similar observational studies have been conducted, this specific approach focusing on psychological outcomes in conjunction with clinical assessments is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients of both sexes and any age, who are referred to the Department of Neurosurgery and Clinical Neurosciences and are candidates for interventional endovascular procedures for any cerebral or spinal pathology, will be included in the study. Exclusion Criteria: * /
Where this trial is running
Milan
- Foundation IRCCS Carlo Besta Neurological Institute — Milan, Italy (Recruiting)
Study contacts
- Study coordinator: Elisa Ciceri, M.D.
- Email: elisa.ciceri@istituto-besta.it
- Phone: 02.2394.2411-2412
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.