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:
2025-12-24 @ 7:09 PM
Ignite Modification Date:
2025-12-24 @ 7:09 PM
NCT ID:
NCT02172703
Eligibility Criteria:
Inclusion Criteria:
* Adult patients, age ≥ 18 years, admitted after TBI or SAH at the Neurosurgical Department, Kantonsspital Aarau, Switzerland.
* Patients under sedation and ICP monitoring
* Informed consent will be obtained from the relatives prior to initiation of the measurements.
* study inclusion/informed consent from relatives possible between hour 24 to 72 after admission to the hospital
Exclusion Criteria:
* Age \< 18 years at study entry.
* Patients with wounds, scars including the front orbital region.
* Perforating or penetrating mechanism of TBI
* Patients with orbital injury or abnormal blood flow in both Ophthalmic Arteries
* Patients with previous retina surgery
* Patients with previous cataract surgery
* Patients with any known ocular condition that may be worsened by sustained eye pressure in the opinion of the subject's ophthalmologist
* Patients with radiological signs of calcification or atheromatose plaques in the internal carotid artery detected by CT or angiography (performed prior and independently of the study)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02172703
Study Brief:
Protocol Section:
NCT02172703