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Evaluation of the effect of royal jelly on the side effects of methylprednisolone treatment

Phase 3
Conditions
Covid 19.
Coronavirus infection, unspecified
U07.1
Registration Number
IRCT20210616051596N1
Lead Sponsor
Shahre-kord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients with positive PCR test who are treated with methylprednisolone.

Exclusion Criteria

Patients with diabetes,
immune deficiency
acute bacterial infectious disease
allergy to bee products

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver function factors (AST, ALT, ALKP, BILD, BILT). Timepoint: Daily. Method of measurement: Blood tet.;Renal function factors (Na, K, Cr and BUN). Timepoint: Daily. Method of measurement: Blood test.;Hematological factors (WBC, Hb, PLT). Timepoint: Daily. Method of measurement: Blood test.;FBS. Timepoint: Daily. Method of measurement: Blood test.;Dose and frequency of need for regular insulin (IR). Timepoint: Daily. Method of measurement: cheklist.;Dosage and frequency of corticosteroids. Timepoint: daily. Method of measurement: cheklist.;Clinical symptoms (chills, sore throat, abdominal pain, diarrhea, dyspnea, cough, shortness of breath). Timepoint: 7 day intervals. Method of measurement: Examination and questions.;Inflammatory factors (ferritin and LDH). Timepoint: 7 day intervals. Method of measurement: Blood test.;Disease severity. Timepoint: daily. Method of measurement: Need medical care, supportive oxygen, need mechanical ventilation.;Spo2. Timepoint: Daily. Method of measurement: Oximetry.
Secondary Outcome Measures
NameTimeMethod
Duration of hospitalization. Timepoint: Duration of hospitalization due to Covid-19. Method of measurement: File review.
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