Eligible study protocols
Identifier | Country | Study design | Arms | Intervention | Comparison | Sample size | Follow-up period |
NCT04357730 | USA | RCT | 2 arms | Alteplase | Standard of care | 50 | 28 days |
NCT04640194 | Austria, Belgium, Brazil, Denmark France, Germany, Italy, Netherlands, Portugal, Russian Federation, Spain | RCT | 3 arms | Alteplase (low dose) on top of standard of care Alteplase (high dose) on top of standard of care | Standard of care | 320 | 28 days |
NCT04505592 | USA | RCT | 2 arms | Tenecteplase | Placebo | 60 | 28 days |
IRCT20200415047080N1 | Iran | RCT | 2 arms | Alteplase | Standard of care | 30 | 28 days |
IRCT20200515047456N1 | Iran | RCT | 3 arms | rtPA | Standard of care | 15 | 30 days |
RCT, randomised controlled trial; rtPA, recombinant tissue plasminogen activator.