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Effect of Nanomicelle Curcumin in pediatric asthma

Evaluation of the Effectiveness of Nanomicelle Curcumin Formulation on Clinical and Spirometry Parameters of Asthma in Children

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191221045837N3
Enrollment
90
Registered
2020-10-24
Start date
2020-11-05
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

asthma. Mild persistent asthma

Interventions

Intervention 1: Intervention group: In the intervention group, asthmatic patients will receive standard treatment of asthma (based on asthma severity and according to the Global Initiative for Asthma

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: Pediatric patients admitted to allergy subspecialized clinic of Akbar hospital 6-12 years old With mild persistant asthma based on Global Initiative for Asthma (GINA) 2019 guideline Informed consent of patient/caregiver

Exclusion criteria

Exclusion criteria: Patients with pulmunary infection Patients with underlying cardiac, hepatic, biliary, renal, or gastrointestinal diseases or allergic rhinitis Patients with smoker parents Patients taking anticoagolant or antiplatelet medications Patients with diabetes

Design outcomes

Primary

MeasureTime frame
Patients' clinical signs score in asthma control questionnaire (c-ACT). Timepoint: At baseline and end of the study (end of the second month). Method of measurement: Asthma Control Questionnaire.;Maximal Mid-Expiratory Flow rate (MMEF25-75). Timepoint: At baseline and end of the study (end of the second month). Method of measurement: spirometry test.;Value of Forced expiratory volume in one second (FEV1). Timepoint: At baseline and end of the study (end of the second month). Method of measurement: spirometry test.;Value of Forced Vital Capacity (FVC). Timepoint: At baseline and end of the study (end of the second month). Method of measurement: spirometry test.;Ratio of Forced expiratory volume in one second (FEV1)/Value of Forced Vital Capacity (FVC). Timepoint: At baseline and end of the study (end of the second month). Method of measurement: spirometry test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZinat Heidari

Mashhad University of Medical Sciences

heidarizn@mums.ac.ir+98 51 3180 1584

Outcome results

None listed

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