Table 2.
Trial Name/Authors (Reference) | Steroid Used, Dosing | Trial Design, Population | Initiation Timing | Duration of Administration (Days) | Main Outcome(s) | Secondary Outcome(s) | Viral Clearance |
---|---|---|---|---|---|---|---|
Tomazini BM et al. CoDEX trial [27] | dexa 20 mg iv × 5 d, then 10 mg dexa × 5 d or until ICU discharge | MC/R/O-L moderate to severe ARDS: SOC vs. SOC + dexa | Not mentioned | ≤10 | Dexa group: mean 6.6 ventilator-free d (95% CI, 5.0–8.2) vs. SOC group: 4.0 ventilator-free d (95% CI, 2.9–5.4), (difference, 2.26; 95% CI, 0.2–4.38; p = 0.04). | D28 no significant difference in: All-cause mortality Clinical status ICU free d MV duration SOFA | NA |
RECOVERY trial [16] | dexa 6 mg/day pos or iv | Controlled/O-L CS vs. SOC | NA | 10 | D28 mortality: 22.9% dexa vs. 25.7% SOC, greater ↓ in pts on MV > O2 and if initiation > 7 d | Time to discharge Need for MV Need for CRRT | NA |