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Effect on Fenoterol Metered Dose Inhaler on the Beta-receptor Population on Lymphocytes in Patients With Bronchial Asthma

Effect of Fenoterol Metered Dose Inhaler (0.1 mg) on the Beta-receptor Population on Lymphocytes and the Clinical Findings Compared With Treatment With DSCG Metered Dose Inhaler in Patients With Bronchial Asthma.

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02177370
Enrollment
19
Registered
2014-06-27
Start date
1990-02-28
Completion date
Unknown
Last updated
2014-07-18

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

Conditions

Asthma

Brief summary

The aim of the study was to compare the effect of fenoterol metered dose inhaler with disodium cromoglycate (DSCG) metered dose inhaler on the lymphocyte β2-receptor population as well as on the clinical findings in patients with bronchial asthma over a two-week period of treatment.

Interventions

DRUGFenoterol MDI
DRUGDSCG MDI

Sponsors

Boehringer Ingelheim
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

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

Inclusion criteria

* sex: male and female * age: 18 years or over * bronchial asthma, diagnosis confirmed by history and positive inhalation challenge test (unspecific challenge with carbachol, PD100SRaw)) * severity of asthma mild to moderate or asthmatic in symptom-free intervals * Raw ≤ 5 cm H2O/l/s * no antiasthmatic treatment in the week (steroid therapy: two weeks) before the start of the study

Exclusion criteria

* clinically significant, concomitant haematological, cardiac, renal, hepatic or metabolic diseases * intercurrent diseases, e.g. severe respiratory infections * patients who cannot do without the following preparations during the 5-week trial: * inhaled/oral steroids * theophylline * antihistamine, antiallergic drugs * inhaled/oral sympathomimetics * anticholinergics

Design outcomes

Primary

MeasureTime frame
Airway resistance (Raw)after 2 weeks
Number of binding sites of the β2 receptors per lymphocytes (BS/LY)after 2 weeks

Outcome results

None listed

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