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All Studies   Meta Analysis    Recent:   
0 0.5 1 1.5 2+ Hospitalization 80% Improvement Relative Risk Recovery 18% Recovery time 8% no CI Probiotics  Hassan et al.  EARLY TREATMENT  RCT Is early treatment with probiotics beneficial for COVID-19? RCT 100 patients in Egypt (July 2021 - August 2022) Lower hospitalization (p=0.2) and improved recovery (p=0.42), not sig. c19early.org Hassan et al., Research Square, June 2023 Favors probiotics Favors control

The effects of probiotic Lactobacillus acidophilus and colchicine on the control of symptoms, duration, and disease progression of mild and moderate cases of COVID-19: A randomized controlled clinical trial

Hassan et al., Research Square, doi:10.21203/rs.3.rs-3049708/v1
Jun 2023  
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Probiotics for COVID-19
17th treatment shown to reduce risk in March 2021
 
*, now known with p = 0.0000013 from 26 studies.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
4,100+ studies for 60+ treatments. c19early.org
RCT 150 patients in Egypt showing no significant difference in outcomes with probiotic lactobacillus acidophilus, although hospitalization was 2% versus 10% for control. SOC included vitamin C, D, and zinc.
The immune effects of probiotics are strain-specific.
Study covers colchicine and probiotics.
risk of hospitalization, 80.0% lower, RR 0.20, p = 0.20, treatment 1 of 50 (2.0%), control 5 of 50 (10.0%), NNT 12.
risk of no recovery, 17.9% lower, RR 0.82, p = 0.42, treatment 23 of 50 (46.0%), control 28 of 50 (56.0%), NNT 10.0.
recovery time, 8.3% lower, relative time 0.92, treatment 50, control 50.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Hassan et al., 13 Jun 2023, Randomized Controlled Trial, Egypt, preprint, 6 authors, study period July 2021 - August 2022. Contact: dr.samar.osama@med.asu.edu.eg.
This PaperProbioticsAll
The effects of probiotic Lactobacillus acidophilus and colchicine on the control of symptoms, duration, and disease progression of mild and moderate cases of COVID-19: A randomized controlled clinical trial
Samar Osama Ahmed Hassan, Ahmed Nour El-Din Hassan, Manal Sabry Mohamed, Mohamed Nabil Badawy Al Ashram, Mina Michael Nesim, Mohamed Farouk Allam
doi:10.21203/rs.3.rs-3049708/v1
Background Coronavirus disease 2019 (COVID-19) is a newly emerging human disease caused by a novel coronavirus, causing a global pandemic crisis. Probiotics and/or colchicine may be considered as options for treatment since they have anti-viral, anti-in ammatory, and immunomodulatory effects. Objective To assess the effectiveness of probiotic supplements (Lactobacillus acidophilus) and colchicine on symptoms, duration, and progression of mild and moderate cases of COVID-19 infection. Methods A three-arm randomized controlled clinical trial was carried out in the triage clinic of the family medicine department at Ain Shams University Hospitals on 150 participants who had been diagnosed as COVID-19 patients with mild and moderate severity. Patients aged below 18 years or above 65 years with any comorbidities, pregnant or lactating females, and severe COVID-19 con rmed cases were excluded. Randomization was done by using sealed envelopes containing codes for intervention or control. Patients are followed up for improvement of their symptoms with no development of new symptoms over the course of two weeks. Results A total of 150 patients with mild and moderate severity of COVID-19 were enrolled in the study, 50 patients in each arm; around one third (34.7%) of the participants were aged between 29 and 39 years; one-quarter (24.7%) were aged between 18 and 28 years and 40.6% were aged 40 years and above. The mean duration of symptoms improvement was 12, 11 and 12 in the colchicine, probiotic, and control groups, respectively. Improvement of in ammatory markers over time occurred in each of the three groups, with no statistically signi cant difference between them. Conclusion Probiotic Lactobacillus acidophilus and colchicine shows no signi cant effect on the symptoms, duration, and progression of mild and moderate cases of COVID-19.
Declarations Author contributions: Each author declares having participated in the activities. Funding: None. Figure 1 See image above for gure legend.
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