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CompletedNCT00115297Updated Mar 14, 2017Results posted

Montelukast for Early Life Wheezing

A Phase 2/3 interventional study of Montelukast and Placebo in Lung Diseases and Asthma, sponsored by University of Massachusetts, Worcester. Completed at 1 site in United States. Open to participants aged 3 Months to 3 Years. Per ClinicalTrials.gov, last updated 2017-03-14.

Sponsored by University of Massachusetts, Worcester · Phase 2/3, Interventional, and Prevention

Phase
Phase 2/3
Study type
Interventional
Enrollment
62
Allocation
Randomized
Ages
3 Months to 3 Years
Sex
All
01

Study summary

This study will determine the effects of montelukast on the duration of wheezing in children 12 months to 3 years of age who visit a physician for care of a wheezing illness. Only patients from the Ankara area of Hacettepe University Medical Center in Turkey will be included in this study.

Read the detailed description

BACKGROUND:

Asthma has a large impact on the children of our society. It is among the most common chronic diseases of childhood and is the leading cause of absenteeism from school. It is unknown as to why more children are having recurrent episodes of wheezing and why some children have asthma while others do not. There is increasing evidence that differences in innate immune responses among children can determine which child will have recurrent wheezing and asthma. While many studies have focused on the factors that initiate innate immune responses, there are relatively few studies of the downstream factors that cause abnormal airway responses. There is evidence that eicosanoid mediators are part of the innate immune response and can function as its effector arm for allergic responses. The ability of leukotrienes and prostaglandins to produce central features of the asthma phenotype is well described and there is emerging evidence that lipoxins facilitate restoration of allergic changes in the airways. This study will test the hypothesis that the balance of airway eicosanoid expression during early-life wheezing illness and the genetically determined capacity to respond will predict recurrent wheezing. Moreover, an intervention to restore a more normal tissue response to this imbalance will reduce symptoms of early-life wheezing and subsequent recurrent episodes.

DESIGN NARRATIVE:

This will be a prospective, double-blind, randomized, placebo-controlled, parallel-group study of the effects of montelukast on the duration of wheezing in children 12 months to 3 years of age who are under the care of a physician for a wheezing illness. Study treatment will be given for 56 days. Participants who are 2 to 3 years old will receive either 5-mg montelukast tablets or matching placebo. Participants who are 12 months to 2 years old will receive 4-mg montelukast granules or matching placebo. The primary outcome parameter of this study will be the number of days that the infant is observed to be free of wheezing by the primary caregiver. The secondary outcome parameters will be the number of wheezing episodes during the treatment period and the rate of recurrent wheezing during the follow-up period. The study, which is a consortium arrangement between the Brigham and Women's Hospital and the Hacettepe University Medical Center in Turkey, will recruit children only from the Ankara area of Hacettepe University Medical Center in Turkey.

This study will be one of three, which include: 1) measuring the airway eicosanoid profiles of pediatric "wheezing" patients 3 months to 3 years old; 2) determining if genetic variants in eicosanoid metabolic and response pathways are associated with recurrent wheezing; and 3) determining how intervention with montelukast (singulair) affects symptoms and the rate of recurrent wheezing.

02

Conditions studied

  • Lung Diseases
  • Asthma
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 62 is below the median of 72 across 2,118 interventional studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

University of Massachusetts, Worcester is the lead sponsor of 288 studies on the registry; 54 are open to participants now.

Of its 25 completed or terminated interventional studies of FDA-regulated products, 18 (72%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Months to 3 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Physician-diagnosed wheezing illness

Exclusion criteria

Exclusion Criteria:

  • Asthma
  • Prematurity
  • Known intolerance to montelukast
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
62 participants (actual)

Study arms

  • Experimental
    Montelukast

    Participants who are 2 to 3 years old received 5-mg montelukast tablets and participants who are 12 months to 2 years old received 4-mg montelukast granules.

    Drug: Montelukast

  • Placebo comparator
    Placebo

    Participants who are 2 to 3 years old received 5-mg montelukast placebo tablets and participants who are 12 months to 2 years old received 4-mg montelukast placebo granules.

    Drug: Placebo

Interventions

  • DrugMontelukast

    Participants who are 2 to 3 years old received 5-mg montelukast tablets and participants who are 12 months to 2 years old received 4-mg montelukast granules.

  • DrugPlacebo

    Participants who were 2 to 3 years old received placebo montelukast tablets and participants who were 12 months to 2 years old received placebo montelukast granules.

06

What researchers measure

Primary outcomes

  1. Number of Wheezing-free Days of Infant (Observed by Primary Caregiver)

    Time frame: First 56 days of study

Secondary outcomes

  1. Wheezing at Day 7

    Time frame: Study day 7

  2. The Number of Participants Requiring Rescue Beta Agonist Use

    Time frame: Measured during the daytime

07

Results

Posted Feb 6, 2017

Participant flow

Recruited from University hospital clinics and inpatient services

Participant flow — Overall Study
MilestoneMonteluksatPlacebo
Started3032
Completed3032
Not completed00

Outcome measures

PrimaryNumber of Wheezing-free Days of Infant (Observed by Primary Caregiver)
Time frame:
First 56 days of study
Reported as:
Median · Days
Number of Wheezing-free Days of Infant (Observed by Primary Caregiver)
DaysMontelukastPlacebo
Number of Wheezing-free Days of Infant (Observed by Primary Caregiver)25.5 (10.8 to 37.0)30.5 (7.5 to 39.8)
SecondaryWheezing at Day 7
Time frame:
Study day 7
Reported as:
Number · participants
Wheezing at Day 7
participantsMontelukastPlacebo
Wheezing at Day 71022
SecondaryThe Number of Participants Requiring Rescue Beta Agonist Use
Time frame:
Measured during the daytime
Reported as:
Number · participants
The Number of Participants Requiring Rescue Beta Agonist Use
participantsMontelukastPlacebo
The Number of Participants Requiring Rescue Beta Agonist Use1526

Adverse events

Collected over Over the 60 day period of active agent or placebo administration. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Montelukast—0/30 (0%)0/30 (0%)
Placebo—0/32 (0%)0/32 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(Months)MontelukastPlaceboTotal
Median13 (8.5 to 19.3)11.5 (8.3 to 20.0)13.0 (9.0 to 20.0)
Sex: Female, Male
Sex: Female, Male(Participants)MontelukastPlaceboTotal
Female111122
Male192140
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)MontelukastPlaceboTotal
Hispanic or Latino000
Not Hispanic or Latino303262
Unknown or Not Reported000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)MontelukastPlaceboTotal
American Indian or Alaska Native000
Asian000
Native Hawaiian or Other Pacific Islander000
Black or African American000
White303262
More than one race000
Unknown or Not Reported000
Region of Enrollment
Region of Enrollment(participants)MontelukastPlaceboTotal
Turkey303262
08

Study locations

1 site
  • University of Massachusetts/UMass Memorial
    Worcester, Massachusetts 01650, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 14, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00115297
Lead sponsor
University of Massachusetts, Worcester
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Craig Lilly (Principal Investigator, University of Massachusetts, Worcester) — Principal investigator
First posted
Jun 22, 2005
Start date
Sep 2004
Primary completion
Oct 2016
Completion
Oct 2016
Results posted
Feb 6, 2017
Last update
Mar 14, 2017

Study contacts

Craig M. Lilly, MD
study chair · University of Massachusetts/UMass Memorial

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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