Serelaxin | heart failure, in acute heart failure | vs placebo | - | - | - | - | - | - | - | - | - | Endpoint | TE [95% CI] | p val | I2 | n | k | trials |
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All cause death | no data | Cardiovascular death | no data | hospitalisation for heart failure | no data | hospitalisation for cardiovascular causes | no data | CV death, MI hospitalization for HF | no data | death or hospitalization | no data | Cardiovascular death or hospital admission for CHF | no data | heart failure death | no data | BNP under treatment | no data | TE: treatment effect; CI: confidence interval; k: nulmber of trials; n: total number of patients Trial | Studied treatment | Control | Patients |
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Pre-RELAX-AHF, 2009 | intravenous relaxin for 48 hours: 10µg/kg daily, 30µg/kg daily, 100µg/kg daily, 250µg/kg daily | placebo | Patients hospitalized with acute heart failure |
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