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Evaluation of the effect of thyme on corona patients

Evaluation of the therapeutic effect of thyme essence in corona patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200506047319N1
Enrollment
100
Registered
2020-05-22
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

New Corona virus infection. ?????????? ?????? ?????

Interventions

Intervention 1: Intervention group: In addition to receiving medication based on hospital protocol, patients receive 15 cc of daily syrup containing 10% thyme essence in three divided doses. The syru

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: People infected by new corona virus Age over 18 years and under 50 years Patients with covid virus 19 hospitalized in Valiasr Hospital

Exclusion criteria

Exclusion criteria: Respiratory diseases Pregnant woman Allergic diseases Dissatisfaction with participating in the study

Design outcomes

Primary

MeasureTime frame
Cough. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Fever. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Runny nose. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Shortness of breath. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Headache. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Muscle pain. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Sore throat. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Anorexia. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Weakness and lethargy. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Questionnaire.;Percentage of people who are tired. Timepoint: At the beginning of the study (before the intervention) and after the intervention. Method of measurement: Multi-Dimensional Fatigue Questionnaire of Asmets (MFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarjes Khavasi

Zanjan University of Medical Sciences

nxavasi@zums.ac.ir+98 24 3315 6393

Outcome results

None listed

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