Effect of Nanomicelle Curcumin in pediatric asthma
Phase 2
Recruiting
- Conditions
- asthma.Mild persistent asthmaJ45.3
- Registration Number
- IRCT20191221045837N3
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method