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The effect of herbal tea on improving respiratory symptoms in patients with Covid-19

The effect of herbal tea (including mallow flower, chicory seeds, sweet violet flower, Melilotus officinalis and Bindii) on improving respiratory symptoms in patients with Covid-19

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200806048318N1
Enrollment
80
Registered
2020-08-20
Start date
2020-09-22
Completion date
Unknown
Last updated
2020-09-07

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 disease

Interventions

Intervention 1: Intervention group: Patients in this group, in addition to receiving routine treatment, will use the herbal tea including mallow flower, chicory seeds, sweet violet flower, Melilotus O

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Positive result of PCR or CT SCAN of COVID-19 disease in accordance with international standards Age 60-15 years Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: Has diseases such as Alzheimer's, Parkinson's, multiple sclerosis, neuromuscular diseases, myasthenia gravis Pregnant women Patients with blood pressure lower than 40/90 mmHg Breathe more or equal to 30 per minute Blood oxygen saturation less than 93% at rest PaO2 to FiO2 ratio less than or equal to 300 mmHg Patients with more than 50% of exudative lesions in 24-48 hours in the lung image

Design outcomes

Primary

MeasureTime frame
Respiratory rate. Timepoint: Before the intervention and the first to fifth days of treatment. Method of measurement: Observation.;Number of coughs. Timepoint: Before the intervention and the first to fifth days of treatment. Method of measurement: Observation.;Percentage of oxygen saturation. Timepoint: Before the intervention and the first to fifth days of treatment. Method of measurement: Pulse Oximeter device.;Shortness of breath. Timepoint: Before the intervention and the first to fifth days of treatment. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Akhveh

Esfahan University of Medical Sciences

arnica.darou@gmail.com+98 31 3312755

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026