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Doxycycline is a safe alternative to Hydroxychloroquine + Azithromycin to prevent clinical worsening and hospitalization in mild COVID-19 patients: An open label randomized clinical trial (DOXYCOV)
Eugene Sobngwi; Sylvain Zemsi; Magellan Guewo-Fokeng; Jean Claude Katte; Charles Kouanfack; Liliane Mfeukeu-Kuate; Armel Zemsi; Yves Wasnyo; Antoinette Assiga-Ntsama; Jean Arnaud Ndi-Manga; Joelle S Tambekou; William Ngatchou; Charlotte Moussi-Omgba; Jean-Claude Mbanya; Pierre Ongolo-Zogo; Pierre-Joseph Fouda.
Afiliación
  • Eugene Sobngwi; University of Yaounde 1
  • Sylvain Zemsi; RSD Institute
  • Magellan Guewo-Fokeng; RSD Institute
  • Jean Claude Katte; RSD Institute
  • Charles Kouanfack; Yaounde Central Hospital
  • Liliane Mfeukeu-Kuate; Yaounde Central Hospital
  • Armel Zemsi; Yaounde Central Hospital
  • Yves Wasnyo; RSD Institute
  • Antoinette Assiga-Ntsama; Yaounde Central Hospital
  • Jean Arnaud Ndi-Manga; RSD Institute
  • Joelle S Tambekou; RSD Institute
  • William Ngatchou; University of Douala, Faculty of Medicine and Pharmaceutical Sciences
  • Charlotte Moussi-Omgba; Ministry of Public Health Cameroon
  • Jean-Claude Mbanya; Yaounde Central Hospital
  • Pierre Ongolo-Zogo; Yaounde Central Hospital
  • Pierre-Joseph Fouda; Yaounde Central Hospital
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21260838
ABSTRACT
ObjectiveWe aimed to compare the safety and efficacy of a doxycycline-based regimen against the national standard guidelines (Hydroxychloroquine plus Azithromycin) for the treatment of mild symptomatic COVID-19. MethodsWe conducted an open-label, randomized, non-inferiority trial, in Cameroon comparing Doxycycline 100mg, twice daily for 7 days versus Hydroxychloroquine, 400 mg daily for 5 days and Azithromycin 500mg at day 1 and 250mg from day 2 through 5, in mild COVID-19 patients. Clinical improvement, biological parameters and adverse events were assessed. The primary outcome was the proportion of clinical cure at day 3, 10 and 30. Non-inferiority was determined by the clinical cure rate between protocols with a 20 percentage points margin. Results194 participants underwent randomization and were treated with Doxycycline (n=97) or Hydroxychloroquine-Azithromycin (n=97). At day 3, 74/92 (80.4%) participants on Doxycycline versus 77/95 (81.1%) on Hydroxychloroquine-Azithromycin -based protocols were asymptomatic (p=0.91). At day 10, 88/92 (95.7%) participants on Doxycycline versus 93/95 (97.9%) on Hydroxychloroquine-Azithromycin were asymptomatic (p=0.44). At day 30 all participants were asymptomatic. SARS-CoV2 PCR was negative at Day 10 in 60/92 (65.2%) participants allocated to Doxycycline and 63/95 (66.3%) participants allocated to Hydroxychloroquine-Azithromycin. None of the participants were admitted for worsening of the disease after treatment initiation. ConclusionDoxycycline 100 mg twice daily for 7 days is as effective and safe as Hydroxychloroquine-Azithromycin, for preventing clinical worsening of mild symptomatic or asymptomatic COVID-19, and achieving virological suppression. Strengths and Limitations[tpltrtarr] This study is one of the first randomized trial, assessing the efficacy and tolerance of Doxycycline to treat COVID-19 [tpltrtarr]It is one of the first to evaluate disease progression and need to hospitalization in mild or asymptomatic COVID-19 [tpltrtarr]Patients will not receive identical treatments [tpltrtarr]Doxycycline has advantages in terms of availability, safety and cost compared to Hydroxychloroquine and Azytromycin [tpltrtarr]Though this study has encounter 7 lost to follow-up, this does not have a major influence on our results [tpltrtarr]These data will assist clinicians in their daily practice, and provide a new tool for the fight against COVID-19
Licencia
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Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Experimental_studies / Prognostic_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Experimental_studies / Prognostic_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint