Study periods | Enrollment | Baseline assessment | Monitoring | 3-months follow-up | Measurements |
---|---|---|---|---|---|
Time | Hospital admission | Study inclusion | Daily after inclusion for max. 14 days postSAH | + 12 weeks after event (+/− 2 weeks) | N/A |
Eligibility Criteria | x | Â | Â | Â | Â |
Patient information & consenting | x | Â | Â | Â | Â |
Demographic/baseline measures | Â | x | Â | Â | Â |
CSF-sampling | Â | Â | x (daily, if EVD/LD) | Â | Â |
aVSP | Â | Â | x (daily, if imaging) | Â | Â |
DCI | Â | Â | x (daily, if imaging) | Â | Â |
DIND | Â | Â | x (daily, if assessable) | Â | Â |
Spasmolysis | Â | Â | x (daily) | Â | Â |
Intracerebroventricular rtPA | Â | Â | x (daily) | Â | Â |
Triple H therapy | Â | Â | x (daily) | Â | Â |
Surgical decompression | Â | Â | x (daily) | Â | Â |
Nimodipine therapy | Â | Â | x (daily) | Â | Â |
CSF infection | Â | Â | x (daily) | Â | Â |
Surgical site infection | Â | Â | x (daily) | Â | Â |
Chronic hydrocephalus | Â | Â | Â | x | Â |
GOSE | Â | Â | Â | x | Â |
mRS | Â | Â | Â | x | Â |
Hematoma volume | Â | Â | Â | Â | x |
CSF-Hb | Â | Â | Â | Â | x |