| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-114 |
Sentence |
denotes |
Sofosbuvir and daclatasvir for the treatment of COVID-19 outpatients: a double-blind, randomized controlled trial. |
| T2 |
115-128 |
Sentence |
denotes |
INTRODUCTION: |
| T3 |
129-226 |
Sentence |
denotes |
Effective treatments are urgently needed to tackle the novel coronavirus disease 2019 (COVID-19). |
| T4 |
227-348 |
Sentence |
denotes |
This trial aims to evaluate sofosbuvir and daclatasvir versus standard care for outpatients with mild COVID-19 infection. |
| T5 |
349-357 |
Sentence |
denotes |
METHODS: |
| T6 |
358-440 |
Sentence |
denotes |
This was a randomized controlled clinical trial in outpatients with mild COVID-19. |
| T7 |
441-596 |
Sentence |
denotes |
Patients were randomized into a treatment arm receiving sofosbuvir/daclatasvir plus hydroxychloroquine or a control arm receiving hydroxychloroquine alone. |
| T8 |
597-681 |
Sentence |
denotes |
The primary endpoint of the trial was symptom alleviation after 7 days of follow-up. |
| T9 |
682-741 |
Sentence |
denotes |
The secondary endpoint of the trial was hospital admission. |
| T10 |
742-826 |
Sentence |
denotes |
Fatigue, dyspnoea and loss of appetite were investigated after 1 month of follow-up. |
| T11 |
827-916 |
Sentence |
denotes |
This study is registered with the IRCT.ir under registration number IRCT20200403046926N1. |
| T12 |
917-925 |
Sentence |
denotes |
RESULTS: |
| T13 |
926-1093 |
Sentence |
denotes |
Between 8 April 2020 and 19 May 2020, 55 patients were recruited and allocated to either the sofosbuvir/daclatasvir treatment arm (n = 27) or the control arm (n = 28). |
| T14 |
1094-1154 |
Sentence |
denotes |
Baseline characteristics were similar across treatment arms. |
| T15 |
1155-1212 |
Sentence |
denotes |
There was no significant difference in symptoms at Day 7. |
| T16 |
1213-1352 |
Sentence |
denotes |
One patient was admitted to hospital in the sofosbuvir/daclatasvir arm and four in the control arm, but the difference was not significant. |
| T17 |
1353-1482 |
Sentence |
denotes |
After 1 month of follow-up, two patients reported fatigue in the sofosbuvir/daclatasvir arm and 16 in the control arm; P < 0.001. |
| T18 |
1483-1495 |
Sentence |
denotes |
CONCLUSIONS: |
| T19 |
1496-1623 |
Sentence |
denotes |
In this study, sofosbuvir/daclatasvir did not significantly alleviate symptoms after 7 days of treatment compared with control. |
| T20 |
1624-1744 |
Sentence |
denotes |
Although fewer hospitalizations were observed in the sofosbuvir/daclatasvir arm, this was not statistically significant. |
| T21 |
1745-1853 |
Sentence |
denotes |
Sofosbuvir/daclatasvir significantly reduced the number of patients with fatigue and dyspnoea after 1 month. |
| T22 |
1854-1897 |
Sentence |
denotes |
Larger, well-designed trials are warranted. |