Id |
Subject |
Object |
Predicate |
Lexical cue |
T193 |
0-379 |
Sentence |
denotes |
Chloroquine, hydroxychloroquine Some proposed mechanisms are the following: increase in the endosomal Ph necessary for the virus/host cell fusion; interference with the glycosylation of cell receptors; immunomodulatory activity • Not available • Comparison of different hydroxychloroquine dosages vs. placebo in three cohorts (outpatients, inpatients, healthcare workers a risk). |
T194 |
380-504 |
Sentence |
denotes |
Double-blind RCT for outpatients and healthcare workers and open-label RCT for inpatients (NCT04329923, not yet recruiting). |
T195 |
505-702 |
Sentence |
denotes |
Primary endpoints: (a) release from quarantine (outpatients, follow-up 14 days); (b) discharge (inpatients, follow-up 14 days); (c) development of COVID-19 (healthcare workers, follow-up 2 months). |
T196 |
703-789 |
Sentence |
denotes |
• Comparison of hydroxychloroquine vs. ascorbic acid in contacts of COVID-19 patients. |
T197 |
790-841 |
Sentence |
denotes |
Double-blind RCT (NCT04328961, not yet recruiting). |
T198 |
842-910 |
Sentence |
denotes |
Primary endpoint: laboratory-confirmed COVID-19 (follow-up 14 days). |
T199 |
911-1047 |
Sentence |
denotes |
• Comparison of tocilizumab plus hydroxychloroquine plus azithromycin vs. tocilizumab plus hydroxychloroquine in patients with COVID-19. |
T200 |
1048-1097 |
Sentence |
denotes |
Open-label RCT (NCT04332094, not yet recruiting). |
T201 |
1098-1325 |
Sentence |
denotes |
Primary endpoints: (a) in-hospital mortality (follow-up 2 weeks); (b) need for mechanical ventilation in the ICU (follow-up 2 weeks).• Comparison of ciclesonide plus hydroxychloroquine vs. ciclesonide in patients with COVID-19. |
T202 |
1326-1375 |
Sentence |
denotes |
Open-label RCT (NCT04330586, not yet recruiting). |
T203 |
1376-1449 |
Sentence |
denotes |
Primary endpoint: SARS-CoV-2 eradication (based on virus load) at day 14. |
T204 |
1450-1576 |
Sentence |
denotes |
• Comparison of hydroxychloroquine vs. placebo in patients with COVID-19 and under biological treatment and/or JAK inhibitors. |
T205 |
1577-1628 |
Sentence |
denotes |
Double-blind RCT (NCT04330495, not yet recruiting). |
T206 |
1629-1839 |
Sentence |
denotes |
Primary endpoints: (a) incidence rate of COVID-19 (follow-up 27 weeks); (b) prevalence of COVID-19 (follow-up 27 weeks); (c) case fatality rate (follow-up 27 weeks); (d) ICU admission rate (follow-up 27 weeks). |
T207 |
1840-1948 |
Sentence |
denotes |
• Comparison of hydroxychloroquine vs. placebo for the prevention of COVID-19 in healthcare workers at risk. |
T208 |
1949-2000 |
Sentence |
denotes |
Double-blind RCT (NCT04328467, not yet recruiting). |
T209 |
2001-2063 |
Sentence |
denotes |
Primary endpoint: prevalence of COVID-19 (follow-up 12 weeks). |
T210 |
2064-2176 |
Sentence |
denotes |
• Comparison of chemoprophylaxis with lopinavir/ritonavir vs. placebo in healthcare workers exposed to COVID-19. |
T211 |
2177-2228 |
Sentence |
denotes |
Double-blind RCT (NCT04328285, not yet recruiting). |
T212 |
2229-2246 |
Sentence |
denotes |
Primary endpoint: |
T213 |
2247-2335 |
Sentence |
denotes |
Occurrence of a symptomatic or asymptomatic SARS-CoV-2 infection (follow-up 2.5 months). |
T214 |
2336-2457 |
Sentence |
denotes |
• Comparison of hydroxychloroquine vs. placebo in symptomatic COVID-19 patients or exposed healthcare workers/households. |
T215 |
2458-2501 |
Sentence |
denotes |
Double-blind RCT (NCT04308668, recruiting). |
T216 |
2502-2649 |
Sentence |
denotes |
Primary endpoints: (a) incidence of symptomatic COVID-19 among asymptomatic participants; (b) severity rating on a 3-point ordinal scale at day 14. |
T217 |
2650-2765 |
Sentence |
denotes |
• Comparison of remdesivir vs. hydroxychloroquine vs. remdesivir plus hydroxychloroquine in patients with COVID-19. |
T218 |
2766-2824 |
Sentence |
denotes |
Open-label adaptive RCT (NCT04321616, not yet recruiting). |
T219 |
2825-2895 |
Sentence |
denotes |
Primary endpoint: all-cause in-hospital mortality (follow-up 3 weeks). |
T220 |
2896-3007 |
Sentence |
denotes |
• Comparison of lopinavir/ritonavir vs. hydroxychloroquine vs. losartan vs. placebos in patients with COVID-19. |
T221 |
3008-3069 |
Sentence |
denotes |
Double-blind, adaptive RCT (NCT04328012, not yet recruiting). |
T222 |
3070-3146 |
Sentence |
denotes |
Primary endpoint: NIAID COVID-19 Ordinal Severity Scale (follow-up 60 days). |
T223 |
3147-3305 |
Sentence |
denotes |
• Comparison of convalescent plasma plus hydroxychloroquine plus azithromycin vs. hydroxychloroquine plus azithromycin in hospitalized patients with COVID-19. |
T224 |
3306-3355 |
Sentence |
denotes |
Open-label RCT (NCT04332835, not yet recruiting). |
T225 |
3356-3535 |
Sentence |
denotes |
Primary endpoints: (a) change in virus load at days 0, 4, 7, 14 and 28; (b) change in IgM COVID-19 titers at days 0, 4, 7, 14 and 28; (c) change in IgG at days 0, 4, 7, 14 and 28. |
T226 |
3536-3705 |
Sentence |
denotes |
• Comparison of lopinavir/ritonavir vs. hydroxychloroquine vs. lopinavir/ritonavir plus interferon beta-1a vs. remdesivir vs. standard of care in patients with COVID-19. |
T227 |
3706-3759 |
Sentence |
denotes |
Double-blind, adaptive RCT (NCT04315948, recruiting). |
T228 |
3760-3831 |
Sentence |
denotes |
Primary endpoint: severity rating on a 7-point ordinal scale at day 15. |