Is the Measured Diameter of the Optic Nerve Sheath by Cerebral Scan in Patients With Early-phase Meningeal Hemorrhage, Due to a Ruptured Aneurysm, a Prognostic 6-month Mortality Factor ?
GAINE
1 other identifier
observational
114
1 country
1
Brief Summary
Sub Arachnoid Hemorrhage (SAH) is a public health concern because of its high incidence (7/100 000 inhab.), its mortality rate (25%), and its morbidity rate (50%).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 21, 2013
CompletedFirst Submitted
Initial submission to the registry
September 5, 2016
CompletedFirst Posted
Study publicly available on registry
September 9, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 19, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 19, 2022
CompletedJune 12, 2026
June 1, 2026
9 years
September 5, 2016
June 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
patient survival
patient survival
month 6
Eligibility Criteria
Patient admitted to the Neurosurgical Urgent Care Unit for SAH following a ruputred aneurysm
You may qualify if:
- Patients 18 years or older
- Patient admitted to the Neurosurgical Urgent Care Unit for SAH following a ruptured aneurysm
- Patients or one of their loved ones providing written informed consent
- Patients with healthcare coverage
You may not qualify if:
- Unavailability of a CTc in the initial phase (within the first 12 hours) or absence of 1-mm slices from the scan
- Trauma to the optic globe or optic nerve pathology
- Preexisting anomalies of ICP or history of neurosurgical cerebral pathologies
- SAH of non aneurysm origin (e.g. arterio-venous malformation (AVM), tumor, trauma, sepsis)
- Patients under legal protection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Amiens
Amiens, 80054, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Patrick JEANJEAN, MD
CHU Amiens
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2016
First Posted
September 9, 2016
Study Start
August 21, 2013
Primary Completion
August 19, 2022
Study Completion
August 19, 2022
Last Updated
June 12, 2026
Record last verified: 2026-06