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Impact of a Hospital Pharmacist's Intervention on FENO (Fractional Exhaled Nitric Oxide) in Asthmatic Patients

Study of the Impact of a Hospital Pharmacist's Intervention in Collaboration With Pneumologists on Bronchial Inflammation of Outpatient Asthmatic Patients Seen in University Hospital of Liege

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03093363
Enrollment
68
Registered
2017-03-28
Start date
2016-10-31
Completion date
2017-04-30
Last updated
2017-10-25

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

Conditions

Asthma

Brief summary

The impact of a pharmacist's intervention on asthma control has now been well demonstrated, but its effect on inflammatory markers of FENO (Fractional exhaled nitric oxide) in asthmatic patients has been little studied in the literature. The aim of this study is to investigate the impact of a pharmacist's intervention on FENO in patients seen in clinical practice by a pneumologist in a secondary university center.

Interventions

Pharmacist's intervention with asthmatic patients: * Detailed questionnaire on asthma and treatments (atopy, comorbidities, smoking status, asthma control, adverse effects of treatments, etc.) * Explanation of asthma and inflammation * Explanation of triggers and how to avoid it * Explanation of asthma treatments * Explanation of the inhalation technique with a physical demonstration * Emphasis on treatment adherence * Assessment of comorbidities and their treatment * Emphasis on influenza vaccination

OTHERQuestionnaires for control group

\- Detailed questionnaire on asthma and treatments (atopy, comorbidities, smoking status, asthma control, adverse effects of treatments, etc.)

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Adult asthmatics (definition of asthma: FEV1 \[forced expiratory volume in 1 second\] reversibility of at least 12% and 200 mL after 400 mcg of salbutamol and/or PC20M \[provocative concentration of methacholine causing a 20% fall in FEV1\]\<16 mg/mL) * unchanged or increased dose of inhaled corticosteroids prescribed by the pneumologist at the visit * FENO (fractional exhaled nitric oxide) \> or = 25 ppb

Exclusion criteria

* Treatment with oral corticosteroids to treat an asthma exacerbation within 4 weeks before the visit with the pneumologist

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline FENO (fractional exhaled nitric oxide) at 3 months3 monthsFractional exhaled nitric oxide

Secondary

MeasureTime frameDescription
Change from Baseline FVC (forced vital capacity) at 3 months3 months
Change from Baseline FEV1/FVC at 3 months3 months
Change from Baseline ACQ (Asthma Control Questionnaire) at 3 months3 months
Change from Baseline ACT (Asthma Control Test) at 3 months3 months
Change from Baseline miniAQLQ (Asthma Quality of Life Questionnaire) at 3 months3 months
Change from Baseline MARS (Medication Adherence Report Scale) at 3 months3 monthsMeasure of treatment adherence
Change from Baseline FEV1 (forced expiratory volume in 1 second) at 3 months3 months
Change from Baseline score of the inhalation technique at 3 months3 months
Change from Baseline number of severe exacerbations (during the 3 previous months) at 3 months3 monthsSevere exacerbations are asthma exacerbations requiring oral corticosteroids
Change from Baseline smoking status at 3 months3 monthsSmoking status is recorded as non-smoker, ex-smoker, current smoker
Satisfaction of patients with the pharmacist's intervention, with a scale from 0 to 103 months after intervention
Changes in lifestyle related to asthma (free text field to complete by the patient)3 months after intervention
Change from Baseline MRA (Medication Refill Adherence) at 3 months3 monthsMeasure of treatment adherence

Outcome results

None listed

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