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Assessment and comparison of two standard protocols for management of asthma attack

Assessment and comparison of two standard protocols for management of asthma attack in patients admitted to Imam Khomeini and Golestan Hospitals emergency rooms in Ahwaz, Iran

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20151103024853N3
Enrollment
66
Registered
2018-07-15
Start date
2018-06-22
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Acute asthma attack. Unspecified asthma with (acute) exacerbation

Interventions

Intervention 1: Intervention group: the intervention group were recorded at 0, 20, 40, 60 spirometric values of FEV1 and PEFR were measured and recorded. For each patient to record the values of FEV1

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with clinical and para clinical approved asthma with clinical presentation of acute asthma attack Age: minimum 18 years old and maximum 65 years old

Exclusion criteria

Exclusion criteria: COPD CHF Pneumonia Lung disease Nursing mothers Fever Pregnancy Administration of salbutamol in the last 6 hours

Design outcomes

Primary

MeasureTime frame
Clinical state. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Base on alert status, talking, wizing, use of respiratory muscles.;Forced Expiratory Volum in First Secend (FEV1). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Mililiter with use of Peak Flow Meter.;Peak Expiratory Flow Rate(PEFR). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Mililiter with use of Peak Flow Meter.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: mm Hg.;Pulse Rate. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Rate/Minutes.;Respiratory Rate. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Rate/Minutes.;Saturation of arterial blood oxygen (SO2 %). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Pulse Oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Leila Kouti

Ahvaz University of Medical Sciences

lkouti.pharmacotherapy@gmail.com+98 61 3373 8380

Outcome results

None listed

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