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effect of hony and fenogreek seed product on cough

Investigation of the Honey and the Trigonella foenum-graceum L (fenugreek) seeds product effect on post-infectious subacute cough

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240927063182N1
Enrollment
88
Registered
2024-12-09
Start date
2024-11-10
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

post-infectious subacute cough. Cough

Interventions

Intervention 1: Intervention group: Intervention group: Patients will be divided into two groups of 44 people each, one group being the control group and the second group (the intervention group) will

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with cough after upper respiratory tract infection with small respiratory changes in spirometry diagnosed by a pulmonologist All patients studied received standard cough medicine and the medications used by the patients are the same The condition of the patients is stable The age of the patients is 20 to 60 years Willingness and satisfaction of the individual to participate in the study

Exclusion criteria

Exclusion criteria: Patients with a history of diabetes Patients with a history of allergy to compounds in honey and fenugreek seeds Breastfeeding Pregnancy Patients with cough due to other causes Patients with underlying diseases such as CF, bronchopulmonary dysplasia, heart failure, bronchotracheomalacia, bronchiectasis, pulmonary embolism, sarcoidosis and treatment-resistant hypertension Patients with diagnosis or possibility of lung cancer and other malignancies Patients taking hormonal medications Patients with long-term use of corticosteroids Patients forget 20% of the medication dose in the checklist

Design outcomes

Primary

MeasureTime frame
Cough intensity based on the Leicester Questionnaire and the Visual Cough Scale. Timepoint: Investigation of cough intensity at baseline (before the procedure) and 1, 2 and 3 weeks after starting to take the combination of fenugreek and honey. Method of measurement: Use of the Lester questionnaire, the visual cough scale.

Secondary

MeasureTime frame
Improve cough. Timepoint: At the beginning of the study (before the start of the intervention) and 1, 2 and 3 weeks after starting to consume the combination of fenugreek and honey. Method of measurement: Lester questionnaire and visual cough scale.;Quality of life. Timepoint: At the beginning of the study (before the start of the intervention) and 1, 2 and 3 weeks after starting to consume the combination of fenugreek and honey. Method of measurement: Quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Parisa Jafari

Zanjan University of Medical Sciences

parisa.jafari.1349@gmail.com+98 24 6141 3315

Outcome results

None listed

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