???. Asthma
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, patients, in addition to oxygen, received salbutamol with a dose of 5 mg and Frosemide with a dose of 40 mg with nebuliser Mask.Patients
Sponsors
Karaj University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Satisfaction to participate in the study Asthma diagnosis The incidence of mild to moderate asthma attack (the clinical criterion of asthma 1 to 6) Ability to perform respiratory tests
Exclusion criteria
Exclusion criteria: Start over 10 hours of symptoms History of smoking over 10 pack-year Simultaneous acute illness Pregnancy Beta 2 agonist consumption in 6 hours before referral Pneumonia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First second of forced expiration. Timepoint: Before starting treatment, 15, 30 and 45 minutes. Method of measurement: Bionet SPM-7 Spirometr device.;Peak expiratory flow rate. Timepoint: Before starting treatment, 15, 30 and 45 minutes. Method of measurement: Bionet SPM-7 Spirometr device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate. Timepoint: Before starting treatment, 15, 30 and 45 minutes. Method of measurement: The heart rate per minute by examination.;Respiratory rate. Timepoint: Before starting treatment, 15, 30 and 45 minutes. Method of measurement: The respiratory rate per minute by examination.;Clinical criteria of asthma. Timepoint: Before starting treatment, 15, 30 and 45 minutes. Method of measurement: Clinical Criterion of Asthma (CAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDariush Shiri
Karaj University of Medical Sciences
Outcome results
None listed