2021
DOI: 10.1016/j.jiac.2021.08.021
|View full text |Cite
|
Sign up to set email alerts
|

Single-dose oral ivermectin in mild and moderate COVID-19 (RIVET-COV): A single-centre randomized, placebo-controlled trial

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

2
24
0
1

Year Published

2021
2021
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 40 publications
(30 citation statements)
references
References 18 publications
2
24
0
1
Order By: Relevance
“…A total of 4 RCTs, including 1125 COVID-19 patients, reported an incidence of patients recovered in their studies (Fig. 3 D) [ 19 , 37 , 38 , 42 ]. The pooled log OR was 0.11 (95% CI − 0.22–0.45) with low heterogeneity (I^2 = 13.84%, Tau = 0.02).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…A total of 4 RCTs, including 1125 COVID-19 patients, reported an incidence of patients recovered in their studies (Fig. 3 D) [ 19 , 37 , 38 , 42 ]. The pooled log OR was 0.11 (95% CI − 0.22–0.45) with low heterogeneity (I^2 = 13.84%, Tau = 0.02).…”
Section: Resultsmentioning
confidence: 99%
“…(Fig. 3 G) [ 20 , 42 ]. The pooled SMD was − 0.17 (95% CI − 0.45–0.12) with low heterogeneity (I^2 = 0%, Tau = 0.00) .…”
Section: Resultsmentioning
confidence: 99%
“…See Table 1 for more details. In the randomized controlled study in India ( n = 125) ( Mohan et al, 2021 ), patients hospitalized with mild to moderate COVID-19 were divided into three groups for a single oral formulation of IVM at a dose of 24 mg or 12 mg, or placebo in a 1:1:1 ratio, and it was ultimately found that the IVM group did not significantly increase negative RT-PCR responses. In a randomized controlled study conducted in Spain ( n = 24) ( Chaccour et al, 2021 ), patients received a single oral dose of IVM (400 μg/kg) and placebo, followed by RT-PCR, which revealed no difference in the proportion of PCR-positive patients between the IVM and control groups.…”
Section: Resultsmentioning
confidence: 99%
“…In the study conducted by Popp et al ., 50 the record on the presence of adverse reactions at 10, 14, and 28 days was not conclusive. Mohan et al ., 55 in their study, recorded a frequency of abdominal pain of 11.2%; they did not detect serious adverse events with doses of 12 and 24 mg of ivermectin. Cruciani et al ., 48 in his meta-analysis, describe an estimated frequency between 1% and 2%.…”
Section: Drug Used For Self-medication In Covid-19mentioning
confidence: 83%