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Acute Effect of Salbutamol on Heart Rate and Blood Pressure During Exercise in Patients With Moderate or Severe Asthma and Healthy Subjects

Acute Effect of Salbutamol on Heart Rate and Blood Pressure During Exercise in Patients With Moderate or Severe Asthma and Healthy Subjects: Randomized, Double-blind, and Crossover Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03044938
Enrollment
15
Registered
2017-02-07
Start date
2016-08-06
Completion date
2016-11-21
Last updated
2017-02-07

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

Conditions

Asthma, Heart Rate Fast

Keywords

Asthma, Salbutamol, Exercise, Heart Rate, Blood pressure

Brief summary

Contextualization: Exercise is a common triggers of bronchospasm in patients with asthma and healthy subjects. To prevent these symptoms frequently they have to use Short-Acting Beta2-Agonists. However, the cardiovascular effects of salbutamol during and after exercise remain poorly known. Objective: To evaluate the effect of salbutamol on heart rate and blood pressure during exercise in patients with moderate or severe asthma and healthy individuals. Methods: A randomized, double-blind, crossover study will be conducted which 13 individuals with moderate or severe persistent asthma and 13 healthy individuals aged between 20 to 59 years. Patients will perform a maximal effort test on 2 nonconsecutive days, with either 400mcg Salbutamol or 4 placebo puffs. The order of use of placebo or salbutamol will be drawn. During the protocol, heart rate, blood pressure, perception of exertion and peak expiratory flow will be monitored.

Interventions

DRUGsalbutamol

Salbutamol or albuterol is a short-acting β2 adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and chronic obstructive pulmonary disease.

DRUGPlacebo

Neutral preparation for pharmacological effects, given in substitution of a medicine, for the purpose of provoking or controlling reactions, ger. Of a psychological nature, accompanying such a therapeutic procedure.

Sponsors

University of Sao Paulo General Hospital
CollaboratorOTHER
Universidade Ibirapuera
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Intervention model description

Randomized Clinical trial, controlled, double-blind and crossover

Eligibility

Sex/Gender
ALL
Age
20 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

for asthmatics: * Have the diagnosis of moderate or severe asthma according to the clinical criteria described in the literature * Be between 20 and 59 years of age * Being from the Asthma Assistance and Research Center (NAPA) of University of São Paulo Faculty of Medicine Clinics Hospital * Have treatment at the outpatient clinic for at least 3 months, * Have a stable clinical condition for at least 30 days * Make use of the optimized medicine daily * Read and signed the TCLE approved by the Ethics and Research Committee of the Ibirapuera University (UNIB) under opinion nº 1,574,833

Exclusion criteria

for asthmatics: * Individuals diagnosed with another lung disease, * Have psychiatric, musculoskeletal or cardiovascular diseases, * Being smokers * Being pregnant * Practice regular physical activity. Criterion for inclusion of healthy individuals * Be between 20 and 59 years of age * Healthy individuals * Both genders * Age between 20 and 59 years * Read and signed the TCLE approved by the Ethics and Research Committee of the Ibirapuera University (UNIB) under opinion nº 1,574,833 Criteria for the exclusion of healthy individuals * Pregnant women * Smokers * Psychic diseases * Osteomuscular diseases * Practitioners of regular exercise * Physical Activity Readiness Questionnaire (PAR-Q)

Design outcomes

Primary

MeasureTime frameDescription
Heart rateBaseline up to 1 hour and after 1 week.It is being considered that the asthmatic heart rate will increase after the use of salbutamol and that the increase will remain during and after the exercise, in relation to the placebo intervention. To evaluate this variable, the Polar RS800cx heart rate monitor will be used, where the participant will have his heart beats monitored beat to beat until the end of the protocol.

Secondary

MeasureTime frameDescription
Blood pressureBaseline and for 1 hour and after 1 week again.It is being considered that the systemic arterial pressure (SBP) of the asthmatic will not have significant alteration after the use of salbutamol during and after the exercise. To evaluate this variable, a Solidor manual sphygmomanometer and a supermed stethoscope will be used. The SBP will be measured after 10 minutes of initial rest, 15 minutes after administration of the drug, every 3 minutes during the physical test and every 5 minutes for 20 minutes at rest.
Peak flowBaseline, 15 minutes final and after 1 week.Due to improved airflow brought by the drug, the peak expiratory flow is expected to increase with the use of salbutamol.
Subjective perception of Borg1 hour and after 1 week .The modified borg subjective perception scale will be used, where the perception of effort will be reported by a scale ranging from 0 to 10. The scale will be applied during the stress test every 3 minutes and during the final rest phase.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026