Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:49 AM
Ignite Modification Date:
2025-12-25 @ 2:49 AM
NCT ID:
NCT06032533
Eligibility Criteria:
Inclusion Criteria:
* Aneurysmal subarachnoid hemorrhage confirmed by computed tomography (CT) with aneurysm origin confirmed by computed tomography angiography (CTA) or digital subtraction angiography (DSA)
* Aneurysmal subarachnoid hemorrhage symptom-onset ≤ 3 days
* Aneurysm protected by clipping or coiling
* Independent in daily living before symptom onset (mRS ≤ 2)
Exclusion Criteria:
* Subarachnoid hemorrhage caused by a lesion other than cerebral aneurysm
* Symptomatic vasospasm at the time of enrollment
* Previous cerebral lesion e.g. symptomatic cerebral infarction (\>2cm), multiple sclerosis, symptomatic intracerebral hemorrhage, tumour, prior neurosurgery (excluding prior clipping or coiling of cold aneurysms without complications).
* History of severe peripheral vascular disease or signs of severe peripheral vascular disease on physical examination
* History of deep vein thrombosis or signs of deep vein thrombosis on physical examination
* Kidney involvement or prior kidney disease with an estimated glomerular filtration rate (eGFR) below safe levels for contrast infusion in relation to CT-perfusion.
* Pregnancy (Women of child-bearing age will have serum-Humane Choriogonadotropine taken prior to final inclusion. If pregnancy cannot be ruled out,the patient can't be included. Women with a safe birth control method will be encouraged to use this method during the entire period of active treatment.)
* Concomitant other acute life-threatening medical or surgical condition
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06032533
Study Brief:
Protocol Section:
NCT06032533