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Investigating effect of Spirulina dietary supplementation on COVID-19 disease outcomes in patients admitted to Intensive Care Units

Phase 2
Recruiting
Conditions
COVID-19.
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U07.1
Registration Number
IRCT20200720048139N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
138
Inclusion Criteria

All covid-19 patients confirmed with PCR test admitted to the ICU are entered the trial

Exclusion Criteria

Age less than 18
Women during pregnancy and lactation
Consumers of supplements C, E, Omega 3, Antioxidants in the last 3 months
Patients with severe renal failure
Patients with liver failure last stage (cirrhosis)
Patients with uncontrolled hypertension
Patients who do not have a functioning gastrointestinal tract and have not been prescribed oral or intravenous nutrition
Patients with drug / food allergies

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
IL6. Timepoint: The first and 28th of the study. Method of measurement: Blood Sample method: ELISA ; sensivity 0.06 pg/ml.;ESR (Erythrocyte sedimentation rate). Timepoint: The first and 28th of the study. Method of measurement: Automated Modified Westergren.;CRP. Timepoint: The first and 28th of the study. Method of measurement: Blood sampling- ELISA.;Nutrition Status. Timepoint: the first and 28th of the study. Method of measurement: Nutric-score Questionnaire.;Fever. Timepoint: Daily. Method of measurement: Digital Thermometer.;O2 SATURATION. Timepoint: Duration the stay in ICU. Method of measurement: Pulse Oxymeter.
Secondary Outcome Measures
NameTimeMethod
Duration of Stay in ICU. Timepoint: Since the first day till end of stay in ICU. Method of measurement: OBSERVATION.;Ventilator Free days. Timepoint: During the stay in ICU. Method of measurement: Observation.;Mortality Rate. Timepoint: During the stay in ICU. Method of measurement: Observation.
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