Predicting complications in patients with subarachnoid hemorrhage
R&D of Innovative Technology for Predicting and Early Warning of Delayed Cerebral Ischemia After Subarachnoid Hemorrhage
Vilnius University · NCT06006975
This study is trying to see if certain medical tests and data can help predict complications in patients with subarachnoid hemorrhage to improve their treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 250 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Vilnius University (other) |
| Locations | 1 site (Vilnius) |
| Trial ID | NCT06006975 on ClinicalTrials.gov |
What this trial studies
This observational study aims to predict the clinical outcomes of patients with subarachnoid hemorrhage (SAH) by analyzing clinical data from the early pre-vasospasm phase. It focuses on identifying biomarkers from various imaging techniques, including Computed Tomography (CT) and transcranial Doppler examinations, to forecast the development of cerebral vasospasms and delayed cerebral ischemia. The study will also explore the impact of other clinical data on patient outcomes, with the goal of improving treatment strategies for SAH patients.
Who should consider this trial
Good fit: Ideal candidates for this study are patients diagnosed with subarachnoid hemorrhage who require surgical intervention and routine postoperative care.
Not a fit: Patients with mental disorders, minors, or those currently serving in the military may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better prediction and management of complications in SAH patients, potentially reducing mortality rates.
How similar studies have performed: While there have been studies exploring similar predictive approaches, this specific methodology focusing on multimodal physiological monitoring and CT analysis is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subarachnoid hemorrhage patients who require SAH surgery and post-operative routine treatment. Exclusion Criteria: * persons with mental disorders, but who can give consent to participate in biomedical research; * minors; * students, if their participation in biomedical research is related to studies; * persons living in care institutions; * soldiers during their actual military service; * employees of health care institutions where biomedical research is conducted, subordinate to the researcher;
Where this trial is running
Vilnius
- Vilnius University Hospital Santaros klinikos — Vilnius, Lithuania (RECRUITING)
Study contacts
- Principal investigator: Saulius Rocka, Prof. Dr. — Clinic of Neurology and Neurosurgery, Faculty of Medicine, Vilnius University
- Study coordinator: Saulius Rocka, Prof. Dr.
- Email: saulius.rocka@santa.lt
- Phone: +37068743480
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: Subarachnoid Hemorrhage, Aneurysmal, Vasospasm, Cerebral, Ischemia, Outcome, Fatal, subarachnoid hemorrhage, delayed cerebral ischemia, computed tomography