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Evaluation of the effectiveness of Cyclotide complex herbal syrup in preventing COVID-19 virus in exposed individuals

Pilot clinical trial to evaluate the effectiveness of Herbal Cyclotide complex syrup as a prevention of disease complications in people exposed to COVID-19 virus

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160131026298N4
Enrollment
60
Registered
2020-08-04
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

COVID-19 viral disease. Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: Consumable product includes herbal syrup composed of cyclopeptide fraction with Ziziphus spina-cristi and Pimpinela anisum hydroalcoholic extract and orange peel. T

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: People over the age of 18 who have had close contact with a person with COVID-19 in the last 4 days and signed an informed consent form (close contact is defined as those who live at home with an infected person or depending on their employment situation in Less than two meters away from the infected person.) And have no previous or current history of COVID-19. Age between 18 and 70 years No previous diagnosis of COVID-19 (if possible, test negative for IgG and IgM antibodies.) Absence of symptoms such as fever, body aches, olfactory and taste disturbances, cough, shortness of breath, diarrhea in the last 1 month

Exclusion criteria

Exclusion criteria: Current incidence of COVID-19 is confirmed by PCR and clinical signs. History of autoimmune disease History of rheumatic disease Pregnancy and lactation Age under 18 years People sensitive to any component of the product People who can not follow up. Any clinical reason that may prevent you from entering the study. Do not take two doses of the drug

Design outcomes

Primary

MeasureTime frame
Polymerase chain reaction (PCR) analysis result. Timepoint: At the beginning of the intervention and the day 14. Method of measurement: Polymerase chain reaction (PCR) analysis.;Liver function test result. Timepoint: At the beginning of the intervention and the day 14. Method of measurement: Measurement of aspartate aminotransferase (AST) and Alanine transaminase (ALT) factors.;Fragment D-dimer test result. Timepoint: At the beginning of the intervention and the day 14. Method of measurement: Blood test - Fragment D-dimer measurement.;Measurement of serum iron. Timepoint: At the beginning of the intervention and the day 14. Method of measurement: Blood test - Total iron binding capacity factor (TIBC) measurement.;COVID-19 Antibodies. Timepoint: At the beginning of the intervention and the day 14. Method of measurement: Measurement of IgG COVID-19 and IgM COVID-19 factors.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShiva Shamshiri

Tehran University of Medical Sciences

shiva.shamshiri90@yahoo.com+98 21 2642 1927

Outcome results

None listed

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