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Acute Effect of Mometasone on Beta-adrenergic Airway and Airway Vascular Relaxation in Severe Asthma

Primary Purpose

Asthma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
placebo
mometasone 400 mcg
mometasone 200 mcg
Sponsored by
University of Miami
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Asthma focused on measuring asthma,, inhaled corticosteroids,, airway blood flow,, mometasone,, albuterol, spirometry

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:Fifteen non-smokers (males and females between the ages of 18 and 65 years) with physician-diagnosed moderate persistent asthma and FEV1 < 75% of predicted.

Exclusion Criteria:Cardiovascular disease and use of cardiovascular medications, pregnancy, use of oral controller medication for asthma (methylxanthines, systemic glucocorticosteroids, leukotriene modifiers), an acute respiratory infection within 4 weeks before enrollment

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Sites / Locations

  • Human Research Laboratory- University of Miami School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm Type

Experimental

Experimental

Placebo Comparator

Placebo Comparator

Experimental

Placebo Comparator

Experimental

Experimental

Experimental

Arm Label

mometasone 400 mcg - 30 min

mometasone 400 mcg simultaneous

placebo- 30 min

placebo simultaneous

mometasone 400 mcg - 60 min

placebo- 60 min

mometasone 200 mcg - 30 min

mometasone 200 mcg - 60 min

mometasone 200 mcg simultaneous

Arm Description

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

randomly assigned intervention

Outcomes

Primary Outcome Measures

Albuterol-induced Change in FEV1
FEV1 will be measured before and after inhalation of 180 mcg albuterol.

Secondary Outcome Measures

Albuterol Induced Percent Change in Qaw
Qaw will be measured before and 15 min after albuterol inhalation

Full Information

First Posted
September 27, 2010
Last Updated
October 20, 2017
Sponsor
University of Miami
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT01210170
Brief Title
Acute Effect of Mometasone on Beta-adrenergic Airway and Airway Vascular Relaxation in Severe Asthma
Official Title
Acute Effect of Mometasone Furoate DPI on Beta-adrenergic Airway and Airway Vascular Relaxation in Moderately Severe Asthma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
February 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Miami
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Glucocorticosteroids inhibit the disposal of organic cations by blocking organic cation transporters expressed by non-neuronal cells, thereby interfering with the inactivation of the organic cations by intracellular enzymes. Beta2-adrenergic agonists are organic cations, and the concentration of inhaled beta2-adrenergic agonists at beta2-adrenergic receptor sites on smooth muscle is likely to be increased by inhaled glucocorticosteroids (ICS) by the ICS' effect on the glucocorticosteroid-sensitive organic cation transporters. The investigators have shown in human airway vascular smooth muscle cells that the glucocorticosteroid action on organic cation uptake occurs within minutes, does not involve gene transcription or protein synthesis, is not mediated through classical steroid receptors, and is cell membrane-linked. In the present proposal, the investigators wish to use different single doses of mometasone, a clinically effective ICS, administered with or at different times before albuterol inhalation in subjects with moderate persistent asthma who are obstructed at the time of study. With this approach the investigators will test the hypothesis that a single inhalation of mometasone causes an acute, transient, dose-dependent potentiation of beta2-adrenergic bronchodilation. If the hypothesis that a single dose of mometasone acutely potentiates beta2-adrenergic bronchodilation is correct, the results would have a significant impact on treatment strategies involving ICSs and beta2-adrenergic agonists in patients with asthma.
Detailed Description
Fifteen non-smokers (males and females between the ages of 18 and 65 years) with physician-diagnosed moderate persistent asthma will be recruited for the study. The subjects will be allowed to use inhaled controller (including ICS) and rescue medication. At study entry, all asthmatic subjects must be clinically stable, and have a forced pre-bronchodilator one-second expired volume (FEV1) of < 75% predicted. Approval for the protocol will be requested from the University of Miami Institutional Review Board. All subjects will provide written informed consent. Exclusion criteria: Cardiovascular disease and use of cardiovascular medications Pregnancy Use of oral controller medication for asthma (methylxanthines, systemic glucocorticosteroids, leukotriene modifiers) An acute respiratory infection within 4 weeks before enrollment. Each subject will make 8 visits to the research laboratory. Procedures: Visit 1 (screening visit): On this visit, after having signed the consent form, the subjects will perform spirometry before and 15 min after inhaling 180 µg albuterol from a HFA-MDI using a spacer. Visit 2-8:Subjects that qualify for the study will be asked to return for 7 more visits for the following treatment protocols: Inhalation of 400 µg mometasone 30 min before inhalation of 180 µg albuterol Inhalation of mometasone placebo 30 min before inhalation of 180 µg albuterol Simultaneous inhalation of 400 µg mometasone and 180 µg albuterol Simultaneous inhalation of mometasone placebo and 180 µg albuterol Systemic blood pressure, pulse, O2 saturation, spirometry and airway blood flow ( Qaw) will be measured before mometasone or placebo inhalation, and before and 15 min after albuterol inhalation except on the day when mometasone and albuterol are co-administered; on that day the measurements will be made before and 15 min after the mometasone/albuterol co-administration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
asthma,, inhaled corticosteroids,, airway blood flow,, mometasone,, albuterol, spirometry

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
mometasone 400 mcg - 30 min
Arm Type
Experimental
Arm Description
randomly assigned intervention
Arm Title
mometasone 400 mcg simultaneous
Arm Type
Experimental
Arm Description
randomly assigned intervention
Arm Title
placebo- 30 min
Arm Type
Placebo Comparator
Arm Description
randomly assigned intervention
Arm Title
placebo simultaneous
Arm Type
Placebo Comparator
Arm Description
randomly assigned intervention
Arm Title
mometasone 400 mcg - 60 min
Arm Type
Experimental
Arm Description
randomly assigned intervention
Arm Title
placebo- 60 min
Arm Type
Placebo Comparator
Arm Description
randomly assigned intervention
Arm Title
mometasone 200 mcg - 30 min
Arm Type
Experimental
Arm Description
randomly assigned intervention
Arm Title
mometasone 200 mcg - 60 min
Arm Type
Experimental
Arm Description
randomly assigned intervention
Arm Title
mometasone 200 mcg simultaneous
Arm Type
Experimental
Arm Description
randomly assigned intervention
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
Asmanex placebo
Intervention Description
placebo inhalation before albuterol.
Intervention Type
Drug
Intervention Name(s)
mometasone 400 mcg
Other Intervention Name(s)
Asmanex
Intervention Description
mometasone inhalation before albuterol.
Intervention Type
Drug
Intervention Name(s)
mometasone 200 mcg
Other Intervention Name(s)
Asmanex
Intervention Description
200ug mometasone before albuterol.
Primary Outcome Measure Information:
Title
Albuterol-induced Change in FEV1
Description
FEV1 will be measured before and after inhalation of 180 mcg albuterol.
Time Frame
15 minutes after albuterol inhalation
Secondary Outcome Measure Information:
Title
Albuterol Induced Percent Change in Qaw
Description
Qaw will be measured before and 15 min after albuterol inhalation
Time Frame
change in Qaw 15 minutes after albuterol inhalation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:Fifteen non-smokers (males and females between the ages of 18 and 65 years) with physician-diagnosed moderate persistent asthma and FEV1 < 75% of predicted. Exclusion Criteria:Cardiovascular disease and use of cardiovascular medications, pregnancy, use of oral controller medication for asthma (methylxanthines, systemic glucocorticosteroids, leukotriene modifiers), an acute respiratory infection within 4 weeks before enrollment -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam Wanner
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
Human Research Laboratory- University of Miami School of Medicine
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25611803
Citation
Mendes ES, Cadet L, Arana J, Wanner A. Acute effect of an inhaled glucocorticosteroid on albuterol-induced bronchodilation in patients with moderately severe asthma. Chest. 2015 Apr;147(4):1037-1042. doi: 10.1378/chest.14-1742.
Results Reference
derived

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Acute Effect of Mometasone on Beta-adrenergic Airway and Airway Vascular Relaxation in Severe Asthma

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