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Almond porridge, grape extract, and pea syrup for treatment of Covid-19

Phase 3
Recruiting
Conditions
COVID-19.
COVID-19, virus identified
U07.1
Registration Number
IRCT20220228054150N1
Lead Sponsor
Artesh University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
160
Inclusion Criteria

Age between 18 and 65 years
Conscious consent to participate in the study
positive PCR test and lung involvement on CT scan and positive clinical signs including fever greater than 38 degrees or hot flashes with at least one of the symptoms of dry cough, 24 Respiratory rate per minute, headache or body aches, weakness and lethargy, anosmia (olfactory disorder) or taste disturbances and anorexia Absence of respiratory distress
Candidates for hospitalization

Exclusion Criteria

admission to the intensive care unit
patients with intubation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The Fatigue Assessment Scale (FAS) score. Timepoint: 0, 3, 6 months after treatment. Method of measurement: The Fatigue Assessment Scale (FAS).;Hospital stay. Timepoint: after the initiation of treatment till discharge from hospital. Method of measurement: heath records.
Secondary Outcome Measures
NameTimeMethod
ESR, CRP. Timepoint: during addmision. Method of measurement: laboratory measurement using electroimmunoassay (EIA).
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