Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Efficacy of pragmatic same-day ring prophylaxis for adult individuals exposed to SARS-CoV-2 in Switzerland (COPEP): protocol of an open-label cluster randomised trial.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • معلومة اضافية
    • الموضوع:
      2020
    • Collection:
      Université de Lausanne (UNIL): Serval - Serveur académique lausannois
    • نبذة مختصرة :
      Lopinavir/ritonavir (LPV/r) has been proposed as repurposed drugs for pre-exposure and postexposure prophylaxis as well as therapy of COVID-19. Coronavirus postexposure prophylaxis (COPEP) trial aims at assessing their efficacy as postexposure ring-prophylaxis among adults exposed to SARS-CoV-2. COPEP is a two-arm open-label cluster-randomised trial conducted in three cantons of Switzerland. Asymptomatic contacts (≥16 years) of individuals diagnosed with COVID-19 will be randomised (2:1) to either LPV/r (400 mg/100 mg two times per day) for 5 days, or a standard of care arm (no treatment). Asymptomatic individuals may be either SARS-CoV-2 positive or negative. Contacts living in the single household will form a cluster and will be randomised into the same arm. All participants will be followed-up for 21 days and undergo daily monitoring for COVID-19 symptoms. The primary endpoint is 21-day incidence of laboratory-confirmed COVID-19 with ≥1 compatible symptom, analysed in an intention-to-treat (ITT) analysis. The secondary endpoints include the 21-day incidence of COVID-19 as well as SARS-CoV-2 infection in a modified ITT analysis, excluding participants who had a positive SARS-CoV-2 RT-PCR from oropharyngeal swab and/or a positive SARS-CoV-2 IgG serology at baseline. Assuming a 21-day incidence for COVID-19 of 20% among contacts without postexposure chemoprophylaxis, to detect a relative risk reduction of 60% (ie, translating in an absolute reduction from 20% to 8%), with a power of 80%, an alpha of 5%. Accounting for design effect of cluster design of circa 1.1, we plan to enrol 200 participants to the LPV/r arm and 100 to the standard of care arm, 300 participants in total. Ethics approval has been granted by the Commission Cantonale d'Ethique de la Recherche, Ethikkommission Nordwest- und Zentralschweiz and Comitato Etico Cantonale (ref 2020-00864) and Swissmedic (2020DR3056). Results from this trial will be disseminated via journal articles and presentations at national and international conferences. ...
    • File Description:
      application/pdf
    • ISSN:
      2044-6055
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/33184083; info:eu-repo/semantics/altIdentifier/eissn/2044-6055; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_395E5B616F523; https://serval.unil.ch/notice/serval:BIB_395E5B616F52; urn:issn:2044-6055; https://serval.unil.ch/resource/serval:BIB_395E5B616F52.P001/REF.pdf; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_395E5B616F523
    • الرقم المعرف:
      10.1136/bmjopen-2020-040110
    • Rights:
      info:eu-repo/semantics/openAccess ; CC BY-NC 4.0 ; https://creativecommons.org/licenses/by-nc/4.0/
    • الرقم المعرف:
      edsbas.30A4C79D