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Beta Blockers for the Treatment of Asthma

Evaluation of Beta Blockers for the Treatment of Asthma. A Randomised Controlled Trial of Propranolol

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01074853
Enrollment
18
Registered
2010-02-24
Start date
2010-05-31
Completion date
2012-03-31
Last updated
2019-04-12

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

Conditions

Asthma

Brief summary

Current asthma medicines include inhalers. A common inhaler used in asthma is called a beta-agonist (for example salbutamol). They improve asthma symptoms by stimulating areas in the human airway resulting in widening of the human airway. Although these drugs are useful after the first dose, longterm use can cause worsening asthma symptoms. Beta-blockers are the complete opposite type of medication. Just now they are avoided in patients with asthma as after the first dose they can cause airway narrowing and cause an asthma attack. New research has suggested that long term use of beta-blockers can reduce airway inflammation which can improve asthma control and improve symptoms. This research was done in asthmatic patients who didn't need inhaled steroids to control their asthma. What the investigators want to do is see if the same benefit of beta-blocker use is asthma can be seen in people who take inhaled steroids.

Interventions

DRUGpropranolol

10mg twice daily escalated to 80mg once daily

DRUGplacebo

Matched placebo

Sponsors

Chief Scientist Office of the Scottish Government
CollaboratorOTHER_GOV
University of Dundee
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male and female volunteers with stable mild intermittent or mild persistent asthma. * Stable defined as: FEV1 (Forced Expiratory Volume in 1second) \>80% predicted with diurnal FEV1 variation \<30% when LABA (Long Acting Beta Agonist) washed out. * Methacholine PC20 \<4mg/ml. * Ability to perform spirometry, IOS (Impulse Oscillometry), bronchial challenge and all domiciliary measurements. * Ability to obtain Informed consent. * Mild to Moderate Asthmatics taking ≤1000μg BDP (Beclomethasone Diproprionate) per day or equivalent. * Withhold LABAs for 1 week prior to study.

Exclusion criteria

* Uncontrolled symptoms of asthma. * Resting BP (Blood Pressure) \<110 systolic or HR (Heart Rate)\<60. * Pregnancy or lactation. * Known or suspected sensitivity to the IMP (Investigational Medicinal Product)(s). * Inability to comply with protocol. * Any degree of heart block. * Rate limiting medication including β blockers, rate limiting Calcium - Channel Blockers and Amiodarone. * Any other clinically significant medical condition that may either endanger the health or safety of the participant, or jeopardise the protocol. * An asthma exacerbation within the last 6 months.

Design outcomes

Primary

MeasureTime frame
To establish effects of chronic dosing with 'beta-blockers' on airway tone and hyperreactivity in mild asthmatics.6 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026