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The effect of compound "Ma-ol-asal" of chronic obstructive pulmonary disease (COPD) patients

The effect of compound "Ma-ol-asal" on clinical manifestations and quality of life of chronic obstructive pulmonary disease (COPD) patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190217042737N2
Enrollment
76
Registered
2020-04-04
Start date
2018-03-21
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD). Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: Intervention group: Oral syrup,compound "Ma-ol-asal Syrup contains honey, ginger, cinnamon, cardamom, saffron, Alpinia officinarum, oral syrup (250ml),10 ml three times a day,for 8 we

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients with COPD referring to the lung clinic People who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: Very severe COPD require hospitalization Underlying illnesses, such as CF, Broncho-pulmonary dysplasia, heart failure, broncho-tracheomalacia, bronchiectasis, pulmonary embolism and sarcoidosis. Taking drugs such as aspirin, beta-blocker and NSAID. Allergic to any of the components of "Ma-ol-asal"

Design outcomes

Primary

MeasureTime frame
Clinical symptoms. Timepoint: At the beginning of the study (before the intervention) and 8 weeks after commencing consumption of the compound syrup. Method of measurement: CAT questionnaire.;Quality of life. Timepoint: At the beginning of the study (before the intervention) and 8 weeks after commencing consumption of the compound syrup. Method of measurement: The St George's respiratory questionnaire.

Secondary

MeasureTime frame
Respiratory test changes in FEV1, FEV1 / FVC. Timepoint: At the beginning of the study (before the intervention) and 8 weeks after commencement of the administration of the compound syrup. Method of measurement: Pulmonary functional test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Poursaleh

Shahid Beheshti University of Medical Sciences

z_poursaleh@yahoo.com+98 21 8248 2503

Outcome results

None listed

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