Fight INflammation to Improve outcome after aneurysmal Subarachnoid HEmorRhage (FINISHER) trial: Study protocol for a randomized controlled trial.
Humans
Subarachnoid Hemorrhage
/ complications
Prospective Studies
Treatment Outcome
Stroke
/ complications
Brain Ischemia
/ complications
Cerebral Infarction
/ complications
Inflammation
/ complications
Dexamethasone
/ therapeutic use
Vasospasm, Intracranial
/ prevention & control
Randomized Controlled Trials as Topic
Multicenter Studies as Topic
Clinical Trials, Phase III as Topic
Dexamethasone
aneurysm
clinical trail
glucocorticoid
inflammation
subarachnoid hemorrhage
Journal
International journal of stroke : official journal of the International Stroke Society
ISSN: 1747-4949
Titre abrégé: Int J Stroke
Pays: United States
ID NLM: 101274068
Informations de publication
Date de publication:
02 2023
02 2023
Historique:
pubmed:
2
4
2022
medline:
1
2
2023
entrez:
1
4
2022
Statut:
ppublish
Résumé
Aneurysmal subarachnoid hemorrhage (SAH) has high morbidity and mortality. While the primary injury results from the initial bleeding cannot currently be influenced, secondary injury through vasospasm and delayed cerebral ischemia worsens outcome and might be a target for interventions to improve outcome. To date, beside the aneurysm treatment to prevent re-bleeding and the administration of oral nimodipine, there is no therapy available, so novel treatment concepts are needed. Evidence suggests that inflammation contributes to delayed cerebral ischemia and poor outcome in SAH. Some studies suggest a beneficial effect of anti-inflammatory glucocorticoids, but there are no data from randomized controlled trials examining the efficacy of glucocorticoids. Therefore, current guidelines do not recommend the use of glucocorticoids in SAH. The Fight INflammation to Improve outcome after aneurysmal Subarachnoid HEmorRhage (FINISHER) trial aims to determine whether dexamethasone improves outcome in a clinically relevant endpoint in SAH patients. FINISHER is a multicenter, prospective, randomized, double-blinded, placebo-controlled clinical phase III trial which is testing the outcome and safety of anti-inflammatory treatment with dexamethasone in SAH patients. In all, 334 patients will be randomized to either dexamethasone or placebo within 48 h after SAH. The dexamethasone dose is 8 mg tds for days 1-7 and then 8 mg od for days 8-21. The primary outcome is the modified Rankin Scale (mRS) at 6 months, which is dichotomized to favorable (mRS 0-3) versus unfavorable (mRS 4-6). The results of this study will provide the first phase III evidence as to whether dexamethasone improves outcome in SAH.
Identifiants
pubmed: 35361026
doi: 10.1177/17474930221093501
doi:
Substances chimiques
Dexamethasone
7S5I7G3JQL
Banques de données
ClinicalTrials.gov
['NCT05132920']
EudraCT
['2021-000732-54']
Types de publication
Clinical Trial Protocol
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM