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Completed

NCT Number: NCT00935415

Time-Effect of Montelukast Protection

The aim of this study is to verify MNT time of onset of protection against EIB in asthmatic children by evaluating different time intervals between dosing and challenge, after a single-dose and after three days of once a day MNT administration.

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Key information

Age range

6 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Pediatric Dept Hospital of Bolzano

Bolzano, Italy

About this study

Within few days after a baseline exercise challenge, children was randomized to a double blind, placebo-controlled, three day doses, crossover study design. In practice each eligible patient was randomized by a computer-generated schedule to receive in sequence double-blind treatments with placebo or MNT (5 mg). Patients in sequence 1 received MNT, then crossed over to matching placebo; vice versa the case was for patients in sequence 2. Placebo and active treatments were separated by a 7-10 day wash-out period. Each child was assigned to one out of seven groups in order to perform the exercise challenge at different time intervals from drug administration which occurred always at 8.00 A.M. On day one the challenge was performed in the different groups 1, 2, 3, 4, 5, 6, and 8 hours after drug administration, respectively. Then treatment was continued as a single day dose for three consecutive days and a third challenge was then performed at the same time of the day.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • children with exercise-induced asthma

Exclusion criteria

  • viral infections
  • montelukast treatment

Treatment and study plan

Montelukast

Drug

Montelukast 5 mg

Other names: Singulair

Placebo

Drug

capsules of matching placebo

Primary outcomes

  1. maximal percentage fall in FEV1 after exercise test from the baseline value

    Time frame: at the first and at the third day of single day drug administration

Secondary outcomes

  1. clinical protection

    Time frame: at the first and at the third day of single day drug administration

Sponsors and collaborators

Lead sponsor

Universita di Verona

Other

Registry information

Official study title

Time-Effect of Montelukast on Protection Against Exercise-Induced Bronchoconstriction

Acronym: TEMPE

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Jul 9, 2009
Registry last updated
Jul 9, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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