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. 2022 Jun 21;2022(6):CD015017. doi: 10.1002/14651858.CD015017.pub3
Study Reason for exclusion
Abd‐Elsalam 2021 Retrospective trial registration
Ahmed 2020 No trial registration
Babalola 2021 Active comparator: ivermectin compared to a control (lopinavir/ritonavir) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect
Behera 2020 Irrelevant study design: case‐control study
Biber 2021 Retrospective trial registration
Cadegiani 2020 Irrelevant study design: historical control group, i.e. not RCT
Camprubi 2020 Irrelevant study design: retrospective study
Carvallo 2020 Irrelevant study design: prospective cohort study; additionally ivermectin was administered in combination with other active drugs with unknown influence on COVID‐19
Chachar 2020 Retrospective trial registration
Chahla 2021a Combined intervention: ivermectin administered in combination with another active substance (iota‐carrageenan) with unknown influence on prevention of COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Chahla 2021b Irrelevant study design: cluster‐randomized trial
Chowdhury 2021 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect. Additionally, the study used an active comparator with unproven efficacy (hydroxychloroquine + azithromycin).
CTRI/2020/08/027282 Active comparator: ivermectin compared to a control (vitamin supplements) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
CTRI/2020/08/027394 Active comparator: ivermectin compared to a control (chloroquine/azithromycin/vitamin supplements) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
CTRI/2020/10/028335 Active comparator: ivermectin was compared to a control (tinefcon) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect. Additionally,ivermectin was administered in combination with another active drug (hydroxychloroquine) with unknown influence on COVID‐19.
CTRI/2021/03/031665 Active comparator: ivermectin compared to a control (vitamin C) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Elgazzar 2020 Active comparator (treatment arm): ivermectin was compared to a control (hydroxychloroquine) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Irrelevant population (prevention arm): participants investigated formed a distinguishable group with both pre‐exposure and postexposure risk. No examination on possible infection that had already taken place at randomization.
Study retracted due to ethical concerns on 14 July 2021
Faisal 2020 No trial registration; further author request sent (unclear study design, the term "cross‐sectional study" is used, which indicates that it is not a RCT); no clarifying response received from the author
Galan 2021 Active comparator: ivermectin compared to control arms (hydroxychloroquine/chloroquine) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Gorial 2020 Irrelevant study design: historical control group, i.e. not RCT
Hashim 2020 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
IRCT20180922041089N4 Irrelevant population: study plans to also include participants with diagnosis of COVID‐19 based on suspect CT scan without PCR or antigen test confirmation.
IRCT20200408046987N2 Combined intervention: ivermectin administered in combination with another active drug (sofosbuvir/daclatasvir) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Kishoria 2020 No trial registration
Lima‐Morales 2021 Irrelevant study design: prospective cohort study; additionallyivermectin was administered in combination with other active drugs (azithromycin, montelukast, aspirin) with unknown influence on COVID‐19.
Mahmud 2021 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Morgenstern 2020 Irrelevant study design: retrospective study
Mustaq 2021 Irrelevant study design: quasi‐experimental study
NCT04345419 Irrelevant intervention: registry entry changed investigated intervention from ivermectin to remdesivir.
NCT04360356 Combined intervention: ivermectin administered in combination with another active drug (nitazoxanide) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04373824 Irrelevant study design: non‐randomized study
NCT04374279 Irrelevant intervention: registry entry changed investigated intervention from ivermectin to only bicalutamide.
NCT04382846 Irrelevant intervention: registry entry changed investigated intervention from ivermectin to only nitazoxanide.
NCT04392427 Combined intervention: ivermectin administered in combination with another active drug (nitazoxanide/ribavirin) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04435587 Active comparator: ivermectin was compared to a control (darunavir/ritonavir/hydroxychloroquine) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04447235 Combined intervention: ivermectin administered in combination with another active drug (losartan) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04482686 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04530474 Irrelevant population: study plans to include participants with diagnosis of COVID‐19 only based on suspected symptoms without PCR or antigen test confirmation.
NCT04551755 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04703608 Irrelevant population: study plans to also include participants with diagnosis of COVID‐19 based on suspect clinical or radiological symptoms without PCR or antigen test confirmation.
NCT04723459 Irrelevant intervention: study plans to investigate ivermectin in impregnated masks, not its systemic effect in the human body.
NCT04768179 Combined intervention: ivermectin administered in combination with another active drug (aspirin) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
NCT04937569 Irrelevant study design: prospective cohort study
NCT04951362 Irrelevant population: participants investigated are in a post‐infection state. No examination on effect on acute COVID‐19.
Niaee 2021 Irrelevant population: study included around 30% of SARS‐CoV‐2‐negative participants, which we did not consider appropriate to include into evidence regarding treatment of COVID‐19.
Furhter expressions of concerns regarding the study's design were published.
Okumuş 2021 Retrospective trial registration
Ozer 2021 Irrelevant study design: observational study
Podder 2020 No trial registration
Rajter 2021 Irrelevant study design: retrospective study.
Samaha 2021 Retraction notice
Seet 2021 Active comparator: ivermectin compared to control arms (hydroxychloroquine/povidone‐iodine/vitamin supplements) with unknown influence on prevention of COVID‐19, which we did not consider eligible to determine ivermectin's true effect.
Shah Bukhari 2021 Retrospective trial registration
Shahbaznejad 2021 Irrelevant population: study included 76.8% participants with unknown or negative SARS‐CoV‐2 status, which we did not consider appropriate to include in evidence regarding treatment of COVID‐19.
Shouman 2021 Irrelevant study design: author request sent (even though the register entry and study protocol use the term "randomization", the method of assignment described in the study protocol does not seem to fulfil randomization criteria); response received from the author revealed that the study was not a RCT
Spoorthi 2020 Combined intervention: ivermectin administered in combination with another active drug (doxycycline) with unknown influence on COVID‐19, which we did not consider eligible to determine ivermectin's true effect.

COVID‐19: coronavirus disease 2019; CT: computer tomography; PCR: polymerase chain reaction; RCT: randomized controlled trial.