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. 2021 Jul 28;2021(7):CD015017. doi: 10.1002/14651858.CD015017.pub2

NCT04351347.

Methods
  • Trial design: open‐label RCT with 2 parallel arms

  • Type of record: trial register entry

  • Sample size: 300

  • Setting: NR

  • Country: Egypt

  • Language: English

  • Number of centres: 1

  • Study purpose (treatment, prevention): treatment

  • Trial registration number: NCT04351347

  • Date of registration: 17 April 2020

Participants
  • Inclusion criteria

    • People with COVID‐19

  • Exclusion criteria

    • Allergy or adverse effects to treatment

Interventions
  • Details of intervention

    • Type and dose: ivermectin, no details on dosing and frequency scheme

    • Route of administration: oral

  • Treatment details of control group

    • Standard of care, no details provided

  • Concomitant therapy: NR

Outcomes
  • Primary study outcome

    • Number of participants with improvement or death within 1 month

  • Relevant review outcomes planned

    • Mortality at 30 days

  • Additional study outcomes

    • None

Notes
  • Reason for awaiting classification: unclear if standard of care administered in ivermectin arm; unclear if RT‐PCR confirmed diagnosis at enrolment; unclear healthcare setting

  • Recruitment status: recruiting

  • Prospective completion date: 1 December 2030

  • Date last update posted: 10 March 2021

  • Sponsor/funding: Tanta University