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Montelukast as a Controller of Atopic Syndrome

Montelukast as a Controller of Atopic Syndrome

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00559546
Acronym
MONTAS
Enrollment
61
Registered
2007-11-16
Start date
2007-03-31
Completion date
2007-07-31
Last updated
2007-11-16

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

Conditions

Allergic Conjunctivitis, Asthma, Atopic Eczema, Seasonal Allergic Rhinitis

Brief summary

The purpose of the study is to find out if montelukast can be used to treat the various symptoms of allergic syndrome.

Interventions

DRUGmontelukast

10 mg montelukast tablet each evening for 3 weeks or placebo for 3 weeks in cross-over manner

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
University of Helsinki
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Wheal diameter at least 4 mm in skin-prick test for both birch and timothy * Allergic symptoms in both upper airways (allergic rhinitis) and lower airways (asthma-like symptoms or diagnosed asthma) and at least one of the following: * Allergic conjunctivitis * Atopic eczema * Oral symptoms from vegetables or fruits by cross reactivity to birch * Urticaria in allergen exposure

Exclusion criteria

* Need for regular treatment with glucocorticoids * Current smoking * Other major disease or need for regular drug treatment * Pregnancy

Design outcomes

Primary

MeasureTime frame
Allergic symptoms3 weeks

Secondary

MeasureTime frame
Need for antihistamines or inhaled beta-2-agonists to relieve symptoms3 weeks
Exhaled nitric oxide concentration3 weeks

Countries

Finland

Outcome results

None listed

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