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Time-Effect of Montelukast Protection (TEMPE)

Primary Purpose

Exercise-Induced Asthma, Asthma

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Montelukast
Placebo
Sponsored by
Universita di Verona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Exercise-Induced Asthma focused on measuring asthma, exercise-induced bronchoconstriction, montelukast, clinical protection, children, time effect

Eligibility Criteria

6 Years - 14 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • children with exercise-induced asthma

Exclusion Criteria:

  • viral infections
  • montelukast treatment

Sites / Locations

  • Pediatric Dept Hospital of Bolzano

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Montelukast

Placebo

Arm Description

capsules prepared in blindness

matched placebo

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

clinical protection

Full Information

First Posted
July 7, 2009
Last Updated
July 8, 2009
Sponsor
Universita di Verona
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1. Study Identification

Unique Protocol Identification Number
NCT00935415
Brief Title
Time-Effect of Montelukast Protection
Acronym
TEMPE
Official Title
Time-Effect of Montelukast on Protection Against Exercise-Induced Bronchoconstriction
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
August 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Universita di Verona

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Exercise-Induced Asthma, Asthma
Keywords
asthma, exercise-induced bronchoconstriction, montelukast, clinical protection, children, time effect

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Montelukast
Arm Type
Active Comparator
Arm Description
capsules prepared in blindness
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
matched placebo
Intervention Type
Drug
Intervention Name(s)
Montelukast
Other Intervention Name(s)
Singulair
Intervention Description
Montelukast 5 mg
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
capsules of matching placebo
Primary Outcome Measure Information:
Title
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 Outcome Measure Information:
Title
clinical protection
Time Frame
at the first and at the third day of single day drug administration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: children with exercise-induced asthma Exclusion Criteria: viral infections montelukast treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Attilio Boner, MD
Organizational Affiliation
Universita di Verona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Dept Hospital of Bolzano
City
Bolzano
Country
Italy

12. IPD Sharing Statement

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Time-Effect of Montelukast Protection

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