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Efficacy of Kelofan syrup on COVID-19

Evaluating efficacy of Kelofan syrup, a traditional Iranian medicine product on pulmonary & other clinical and laboratory manifestations of patients with or probable of covid-19

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200405046960N2
Enrollment
60
Registered
2020-05-19
Start date
2020-05-17
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

Condition 1: Covid-19. Condition 2: Covid-19. COVID19, virus identified COVID19, virus not identified

Interventions

Intervention 1: Intervention group: In the intervention group, in addition to the standard treatment, medicinal herbal products will be prescribed.The drug will be given in syrup form. The syrup will

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 18 years old Hospitalized patients withprobable or confirmed COVID-19 based on radiologicalfindings or positive PCR test according to the instructions22of the Ministry of Health Clinically classified as moderateand severe, no need for intubation Written and informedsatisfaction of patients

Exclusion criteria

Exclusion criteria: Liver, kidney and heart failure History of allergies to medicinal herbs Immunodeficiency Uncontrolled hypertension Uncontrolled diabetes Alcohol or drug addiction Patients with transplanted organs Cor Pulmonel Patients Takinganticoagulants, antiarrhythmics, antihypertensives, corticosteroids and immunosuppressants Pregnancy Breast feeding

Design outcomes

Primary

MeasureTime frame
Oxygen saturation. Timepoint: Clinical examination and Pulse Oximetry before starting intervention and regularly during hospitalized. Method of measurement: Pulse Oximeter.;Respiratory Rate. Timepoint: Clinical examination before starting intervention and regularly during hospitalized. Method of measurement: Respiratory Count.

Secondary

MeasureTime frame
C-reactive protein. Timepoint: Intravenous blood testing before starting intervention and during hospitalized. Method of measurement: Venous blood test.;Lymphocytes. Timepoint: Intravenous blood testing before starting intervention and during hospitalized. Method of measurement: Venous blood test.;White Cell blood count. Timepoint: Intravenous blood testing before starting intervention and during hospitalized. Method of measurement: Venous blood test.;Liver enzymes. Timepoint: Intravenous blood testing before starting intervention and during hospitalized. Method of measurement: Venous blood test.;Cough. Timepoint: Clinical examination before starting intervention and regularly during treatment. Method of measurement: Patient follow up.;Fever. Timepoint: Clinical examination before starting intervention and regularly during treatment. Method of measurement: Thermometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRamin Nasimi Doost Azgomi

Ardabil University of Medical Sciences

modir7060@yahoo.com+98 45 3142 2529

Outcome results

None listed

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