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the effect of nanocurcumin and omega_3 supplement in asthma

The effect of nanocurcumin and omega-3 supplementation on quality of life in patients with asthma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191105045340N3
Enrollment
88
Registered
2023-07-11
Start date
2023-08-23
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Asthma. Asthma

Interventions

Intervention 1: Intervention group: Take a 40 mg nanocurcumin capsule (Elixir Nanosina pharmaceutical company) and a 1000 mg omega-3 capsule (Karen pharmaceutical company) daily for 8 weeks. Intervent

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with asthma diagnosed by a doctor Asthma patients with an age range of 15 to 60 years

Exclusion criteria

Exclusion criteria: Users of systemic drugs, NSAIDs, immunosuppressive drugs NSAID users Users of immunosuppressive drugs People with COPD Cardiovascular patients Kidney patients Liver patients Gastrointestinal patients Autoimmune patients suffering from reflexes Lactating lady pregnant lady People addicted to tobacco Allergy and intolerance to curcumin Allergy and intolerance to fish oil Consumption of food supplements and antioxidants from 2 months before and during the study

Design outcomes

Primary

MeasureTime frame
Quality of life of patients with asthma. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: Asthma control questionnaire.;Measurement of airway inflammation in patients with asthma. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: Measurement of exhaled nitric oxide through the FeNo device.

Secondary

MeasureTime frame
Quality of life questionnaire score of patients with asthma. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: Evaluation of the quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh tayebeh rahideh

Iran University of Medical Sciences

tayebeh_rahideh@yahoo.com+98 21 8670 4843

Outcome results

None listed

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