Key result
The FINISHER trial is a phase III study protocol designed to determine whether dexamethasone improves the 6-month functional outcome in patients with aneurysmal subarachnoid hemorrhage.
Why the study?
Inflammation contributes to delayed cerebral ischemia and poor outcome in aneurysmal subarachnoid hemorrhage, but randomized controlled trial data on the efficacy of glucocorticoids are lacking.
Does dexamethasone improve functional outcome at 6 months in patients with aneurysmal subarachnoid hemorrhage?
RCT (n=334)
Double-blind
1:1 ratio stratified by center via permuted blocks
Yes
Does dexamethasone improve functional outcome at 6 months in patients with aneurysmal subarachnoid hemorrhage?
This study protocol describes a phase III trial to evaluate whether dexamethasone improves 6-month functional outcomes in patients with aneurysmal subarachnoid hemorrhage.
RATIONALE: 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. AIM: 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. METHODS AND DESIGN: 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. SAMPLE SIZE ESTIMATES: 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. STUDY OUTCOME: 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). DISCUSSION: The results of this study will provide the first phase III evidence as to whether dexamethasone improves outcome in SAH.
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Güresir et al. (2022) conducted an RCT in Aneurysmal subarachnoid hemorrhage (SAH) (n=334). Dexamethasone vs. Placebo was evaluated on Modified Rankin Scale (mRS) at 6 months, dichotomized to favorable (mRS 0–3) versus unfavorable (mRS 4–6). The FINISHER trial is a phase III study protocol designed to determine whether dexamethasone improves the 6-month functional outcome in patients with aneurysmal subarachnoid hemorrhage.
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