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Effect of oral syrup and intranasal spray of Falcaria Vulgaris plant in patients with Covid-19

Comparison of the effectiveness of oral syrup and intranasal spray of Falcaria Vulgaris plant on patients with Covid-19

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130722014106N9
Enrollment
100
Registered
2021-11-30
Start date
2021-11-22
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

COVID-19. Covid-19

Interventions

Intervention 1: Intervention group: Patients in this group, in addition to receiving standard medications, use a syrup or nasal spray prepared from the mountain ghaziani plant, which is dried under no

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Confirmation of coronavirus infection by CT scan of the chest and PCR test Age 20 to 70 years Willingness to cooperate in the study and completion of informed written consent

Exclusion criteria

Exclusion criteria: pregnant women children Elderly (people over 70) People who use mechanical ventilation People undergoing chemotherapy People who receive corticosteroids are excluded from the study

Design outcomes

Primary

MeasureTime frame
Blood oxygen saturation. Timepoint: At the beginning and end of the study on a regular basis. Method of measurement: Pulse oximeter.;Rate of lung involvement. Timepoint: beginning and end of the study. Method of measurement: computed tomography scan.

Secondary

MeasureTime frame
Number of breaths. Timepoint: At the beginning and end of the study on a regular basis. Method of measurement: Counting breaths per minute.;Body temperature. Timepoint: At the beginning and end of the study on a regular basis. Method of measurement: thermometer and clinical examination.;Dyspnea. Timepoint: At the beginning and end of the study on a regular basis. Method of measurement: clinical examination.;Cough. Timepoint: At the beginning and end of the study on a regular basis. Method of measurement: clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Amiri

Kermanshah University of Medical Sciences

hossein.amirii@yahoo.com008337272049

Outcome results

None listed

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