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Dexmedetomidine in asthma

Comparison clinical efficacy of IV Dexmedetomidine plus nebulized salbutamol in contrast whit nebulized salbutamol alone in management of acute asthma attack

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131118015446N14
Enrollment
60
Registered
2018-06-01
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

Asthma. Asthma

Interventions

The intervention group will receive 0.5 mg ipratropium nubulized (repeated up to 3 doses in every 20 minutes), 5 mg Albuterol inhalation and Prednisolon at the beginning (zero time point). Also, 0.5 m

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: All of patients whit Asthma attack Age between 18-55 years old

Exclusion criteria

Exclusion criteria: Pregnancy Age under 18 and more than 55 years old Smoking more than 10 pack/year Other chronic deaseas

Design outcomes

Primary

MeasureTime frame
PEFR. Timepoint: 0, 30, 60 minutes after treatmen. Method of measurement: Spirometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Motamed

Ahvaz University of Medical Sciences

motamed-h@ajums.ac.ir+98 61 3374 3009

Outcome results

None listed

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