Effect of donkey milk on the new corona virus infectio

Not Applicable

Recruiting

• Conditions: COVID-19.; COVID-19; U07.1

• Registration Number: IRCT20161108030776N3
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 110

Inclusion Criteria

Patients with COVID-19
Mild to moderate disease
Candidates for outpatient treatment based on the protocol of the Ministry of Health
Patients 18-65 years old

Exclusion Criteria

Patients with allergies and asthma
Patients with hypertension
Patients with diabetes
Pregnancy / lactation
Patients with heart failure
Patients with chronic renal failure
Patients undergoing chemotherapy
Patients receiving corticosteroids
Patients with immunodeficiency

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Body temperature. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Mercury thermometer.;Cough (severity-frequency). Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Fiston Scale.;Weakness and lethargy. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Visual analog scale (VAS).;Body pain. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Visual analog scale (VAS).;Breathing speed. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Count the number of breaths per minute.;Diarrhea (watery stools). Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Question from the patient.

Secondary Outcome Measures

Name	Time	Method
Being admitted to the hospital. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: The ratio of the number of cases leading to hospitalization to the total number of patients in each group.;Death rate. Timepoint: Days 0-1-2-3-4-7-14 after the start of the intervention. Method of measurement: Ratio of number of deaths to total patients in each group.