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 @ 12:14 AM
Ignite Modification Date:
2025-12-25 @ 12:14 AM
NCT ID:
NCT02637258
Eligibility Criteria:
Inclusion Criteria:
1-Out-hospital cardiac arrest
Exclusion Criteria:
1. In-hospital cardiac arrest
2. Unstable patients requiring rapid intervention (i.e. emergent surgery, percutaneous coronary intervention)
3. Age \<18
4. Concomitant trauma
5. Pregnancy
6. Any event known to increase ONSD without raised ICP (optic neuritis, arachnoid cysts of optic nerve, optic nerve trauma, anterior orbital mass, cavernous sinus mass)
7. Any event known to increase ONSD with raised ICP \[previously diagnosed intracranial space occupying lesion or tumor, pseudotumor cerebri, conditions causing decreased Cerebrospinal fluid (CSF) reabsorption (venous sinus thrombosis, inflammation, meningitis, subarachnoid hemorrhage)
8. Conditions causing increased production CSF (tumors), ventricular obstructions, cerebral edema, craniosynostosis
9. Anatomical eye malformations preventing the USG examination
10. Previously diagnosed malignity, glaucoma, multiple sclerosis, previously diagnosed terminal stage liver and renal disease,
11. Cardiac arrest secondary to trauma and refusing to give consent to participate
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02637258
Study Brief:
Protocol Section:
NCT02637258