This study is aimed to investigate the effect of Famotidine in the clinical recovery of COVID-19 patients. COVID19 is a worldwide pandemic. Hence SARS-CoV-2 is a novel virus; there is no specific medication against it. Like other countries of the world, Besides antiviral drugs, immunosuppressive agents, and symptomatic therapy like H2 receptor blocker FAMOTIDINE came to the limelight due to its role in reducing the symptoms of COVID-19 patients. The study will include COVID-19 participants to confirm by RT PCR or an HRCT chest. Detail history of each participant with comorbidity will be taken and will be examined carefully. The hospitalized patients admitted to the HDU/ICU units will be enrolled in this study. Critically ill patients who require ventilator support will not be included in this study. The outcome of the Famotidine treatment will be evaluated and compared with a control group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
208
Famotidine; tablet Famotac 20mg oral form.
Chattogram General Hospital
Chittagong, Bangladesh
M. Abdur Rahim Medical College Hospital
Dinājpur, Bangladesh
Time to Clinical Improvement (TTCI)
Time to clinical improvement (TTCI) was defined as time from randomization to National Early Warning Score 2 (NEWS2) Score of ≤2 maintained for 24 Hours.
Time frame: Following randomization 30days.
Time to symptomatic recovery.
Time to Symptomatic recovery was defined as the duration (in days) that required for the relief of the COVID-19 symptoms from the day of hospitalization.
Time frame: Following randomization 30 days.
Mortality Rate
Mortality Rate in percentage in study groups.
Time frame: Following randomization 30 days.
Duration of ICU Stay.
Duration of ICU Stay in days.
Time frame: Following randomization 30 days.
Total hospital stay.
Time from randomization to hospital discharge or "Ready for discharge" (as evidenced by normal body temperature and respiratory rate, and stable oxygen saturation on ambient Air or ≤4L supplemental oxygen).
Time frame: Following randomization 30 days.
Time to clinical failure or death.
Time to clinical failure, defined as the time from randomization to the first occurrence of death, mechanical ventilation or withdrawal (whichever occurs first).
Time frame: Following randomization 30 days.
Time to Viral clearance / COVID-19 recovery.
This was defined as the duration (in days) from the first positive PCR to the first negative PCR (Confirmed by a repeat negative PCR after 7days) for SARS-Cov-2 infection following hospital discharge.
Time frame: Following randomization 60 days.
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