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Effect of bee products on COVID-19

Comparison effect of N-Chromosome royal jelly, propolis, and mixed honey supplementation on clinical and laboratory findings of COVID-19 patients with standard treatment: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200209046427N1
Enrollment
60
Registered
2020-06-07
Start date
2020-05-30
Completion date
Unknown
Last updated
2020-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19 Disease. COVID-19

Interventions

Intervention 1: Control group: Standared treatment for COVID-19 according to hospital protocol for admitted patients. Intervention 2: Intervention group: The case group will be given three products in

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: age between 18 to 90 year old without any psychological problem drug consumption compliance hospital admission during recent 48 hours

Exclusion criteria

Exclusion criteria: Allergy to honey products warfarin usage

Design outcomes

Primary

MeasureTime frame
Dyspnea grade. Timepoint: Dyspnea grade before intervention and daily after starting the intervention. Method of measurement: dyspnea grading according to New York heart association classification.;White blood cells (WBC) count. Timepoint: lab test before intervention and 3, and 7 days after intervention. Method of measurement: lab data assessment by blood sample.;Neutrophil to Lymphocyte count. Timepoint: lab test before intervention and 3, and 7 days after intervention. Method of measurement: lab data assessment by blood sample.;Interleukin-6 (IL-6) Level. Timepoint: lab test before intervention and 3, and 7 days after intervention. Method of measurement: lab data assessment by blood sample.;Anti SARS-Cov-2 IgG Level. Timepoint: one month after intervention. Method of measurement: blood sample.;C-reactive protein (CRP) level. Timepoint: lab test before intervention and 3, and 7 days after intervention. Method of measurement: lab data assessment by blood sample.

Secondary

MeasureTime frame
Duration of hospital stay. Timepoint: duration of hospitalisation. Method of measurement: Hospital records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadi Shafaghi

Shahid Beheshti University of Medical Sciences

shafaghishadi@sbmu.ac.ir+98 21 2712 2522

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026