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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00090142
Other study ID # 0476-275
Secondary ID 2004_009
Status Completed
Phase Phase 3
First received
Last updated
Start date May 2004
Est. completion date October 2004

Study information

Verified date January 2022
Source Organon and Co
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effect of an approved medication being studied in support of a new approach in the prevention of exercise-induced asthma (a worsening of asthma caused by exercise, also known as exercise-induced bronchospasm), in patients who have a history of worsening asthma after exercise.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date October 2004
Est. primary completion date October 2004
Accepts healthy volunteers No
Gender All
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria: - Patients with mild-to-moderate asthma Exclusion Criteria: - Medical history of a lung disorder (other than asthma) or a recent upper respiratory tract infection - Patient is, other than asthma, not in good, stable health - The Primary Investigator will evaluate whether there are other reasons why the patient may not participate

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Comparator: Montelukast
Montelukast 10 mg tablet administered orally as a single witnessed dose before exercise challenge
Comparator: Placebo
Placebo tablet administered orally as a single witnessed dose before exercise challenge

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Organon and Co

References & Publications (1)

Philip G, Villarán C, Pearlman DS, Loeys T, Dass SB, Reiss TF. Protection against exercise-induced bronchoconstriction two hours after a single oral dose of montelukast. J Asthma. 2007 Apr;44(3):213-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum Percent Fall in FEV1 After Exercise Challenge at 2 Hours Post-dose Compared With Pre-exercise Baseline in Patients With Exercise-induced Bronchospasm (EIB) In patients with EIB, the percent change from pre-exercise baseline FEV, to the lowest FEV1 within 60 minutes after exercise challenge (2 hours post-dose). The FEV1 measurement obtained 5 minutes before the exercise challenge was the baseline, and was specific to each exercise challenge. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed 2 hours after a single oral dose
Secondary Number of Patients Requiring ß-Agonist Rescue Medication After Exercise Challenge at 2 Hours Postdose 0-90 minutes after the exercise challenge performed at 2 hours postdose
Secondary Number of Patients Requiring ß-Agonist Rescue Medication After Exercise Challenge at 12 Hours Postdose 0-90 minutes after the exercise challenge performed at 12 hours postdose
Secondary Number of Patients Requiring ß-Agonist Rescue Medication After Exercise Challenge at 24 Hours Postdose 0-90 minutes after the exercise challenge performed at 24 hours postdose
Secondary Maximum Percent Fall in FEV1 After Exercise Challenge at 12 Hours Postdose Compared With Pre-exercise Baseline in Patients With EIB In patients with EIB, the percent change from pre-exercise baseline FEV, to the lowest FEV1 within 60 minutes after exercise challenge (12 hours post-dose). The FEV1 measurement obtained 5 minutes before the exercise challenge was the baseline, and was specific to each exercise challenge. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed 12 hours after a single oral dose
Secondary Maximum Percent Fall in FEV1 After Exercise Challenge at 24 Hours Postdose Compared With Pre-exercise Baseline in Patients With EIB In patients with EIB, the percent change from pre-exercise baseline FEV, to the lowest FEV1 within 60 minutes after exercise challenge (24 hours post-dose). The FEV1 measurement obtained 5 minutes before the exercise challenge was the baseline, and was specific to each exercise challenge. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed 24 hours after a single oral dose
Secondary Area Under the Curve for FEV1 Percent Change From Preexercise Baseline During the 60 Minutes Following Exercise Challenge (AUC 0-60 Min) at 2 Hours Postdose The measure included only the area below the pre-exercise baseline. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed at 2 hours postdose
Secondary Area Under the Curve for FEV1 Percent Change From Preexercise Baseline During the 60 Minutes Following Exercise Challenge (AUC 0-60 Min) at 12 Hours Postdose The measure included only the area below the pre-exercise baseline. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed at 12 hours postdose
Secondary Area Under the Curve for FEV1 Percent Change From Preexercise Baseline During the 60 Minutes Following Exercise Challenge (AUC 0-60min) at 24 Hours Postdose The measure included only the area below the pre-exercise baseline. Pre-exercise baseline measurement and 0-60 minutes after the exercise challenge performed at 24 hours postdose
Secondary Time to Recovery From Maximum Percentage Decrease in FEV1 After Exercise Challenge at 2 Hours Postdose The time to recovery from maximum percent fall is the duration between the time at which the maximum percent fall in FEV1 after exercise challenge occurs and the time when FEV1 returns to within 5% of the preexercise baseline for the first time. Exercise challenge at 2 hours postdose
Secondary Time to Recovery From Maximum Percentage Decrease in FEV1 After Exercise Challenge at 12 Hours Postdose The time to recovery from maximum percent fall is the duration between the time at which the maximum percent fall in FEV1 after exercise challenge occurs and the time when FEV1 returns to within 5% of the preexercise baseline for the first time. Exercise challenge at 12 hours postdose
Secondary Time to Recovery From Maximum Percentage Decrease in FEV1 After Exercise Challenge at 24 Hours Postdose The time to recovery from maximum percent fall is the duration between the time at which the maximum percent fall in FEV1 after exercise challenge occurs and the time when FEV1 returns to within 5% of the preexercise baseline for the first time. Exercise challenge at 24 hours postdose
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