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The Effect of Salmetrol, Tiotropium, and their Combination in Patients with Acute Exacerbation of Chronic Obstructive Pulmonary Disease (COPD)

The Effect of Salmetrol, Tiotropium, and their Combination in Patients with Acute Exacerbation of Chronic Obstructive Pulmonary Disease (COPD)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190123042466N1
Enrollment
108
Registered
2019-04-07
Start date
2019-04-09
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Chronic obstructive pulmonary disease. Other chronic obstructive pulmonary disease

Interventions

Intervention 1: Intervention group: Salmeterol spray will be used three times a day with a dose of 25 micrograms for 15 days. Intervention 2: Intervention group: A thiotropium bromide capsule is given

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with acute exacerbation of COPD Age over 35 years Spirometry or previous histories consistent with chronic obstructive pulmonary disease Patients reporting at least 10 packets of cigarette smoking

Exclusion criteria

Exclusion criteria: Acute coronary syndrome Severe associated comorbidities (cardiac and renal) Patients with a recent history of myocardial infarction Patients with prostate hypertrophy and closed glaucoma Patients with allergic rhinitis or atopy

Design outcomes

Primary

MeasureTime frame
Dyspnea in daily living. Timepoint: At the beginning of the study and 15 days after the start of treatment. Method of measurement: The modified Medical Research Council scale.;Severity of chronic obstructive pulmonary disease. Timepoint: At the beginning of the study and 15 days after the start of treatment. Method of measurement: Chronic obstructive pulmonary disease assessment Test.

Secondary

MeasureTime frame
Arterial blood gas parameters. Timepoint: At the beginning of the study and 15 days after the start of treatment. Method of measurement: Arterial blood gases.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadAli Saba

Kashan University of Medical Sciences

aba-ma@kaums.ac.ir+98 31 5554 0021

Outcome results

None listed

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