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Extra-fine Formoterol/Beclomethasone in Asthmatic Crisis

Primary Purpose

Asthma, Asthmatic Crisis

Status
Unknown status
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Extra fine Formoterol/Beclomethasone
Sponsored by
National Institute of Respiratory Diseases, Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring formoterol/beclomethasone in asthmatic crisis, asthmatic crisis treatment

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • previous asthma diagnosis by physician
  • spirometry with quality grade A, B or C
  • presenting with asthmatic crisis in emergency room

Exclusion Criteria:

  • imminent respiratory arrest
  • respiratory comorbidities (COPD, cystic fibrosis, interstitial lung disease, pneumothorax, bronchiectasis)
  • use of systemic steroids in 3 months previous
  • allergy to steroids
  • Peripheral capillary oxygen saturation (SpO2) less than 88%.

Sites / Locations

  • National Institute of Respiratory Diseases

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Extra fine Formoterol/Beclomethasone

Placebo

Arm Description

Group receiving the drug additional to standard treatment standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline, 0, 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + formoterol/beclomethasone, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes

Group receiving placebo additional to standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline (0), 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + Placebo, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes

Outcomes

Primary Outcome Measures

Pulmonary Function
change in Forced Expiratory Volume in 1 second (FEV1) with respect to basal

Secondary Outcome Measures

Need for hospitalization
Change in perception of dyspnea
change in Borg and Transitional Dyspnea Index
Biomarkers of inflammation
change in C- reactive protein, TNF-alpha, eosinophils
interleukins
change in eosinophilic and non eosinophilic interleukins (IL-4, IL-5, IL-13, IL-17, IL-33)

Full Information

First Posted
January 14, 2015
Last Updated
April 1, 2015
Sponsor
National Institute of Respiratory Diseases, Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT02345993
Brief Title
Extra-fine Formoterol/Beclomethasone in Asthmatic Crisis
Official Title
Extra-fine Formoterol/Beclomethasone in the Treatment of Asthmatic Crisis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (undefined)
Primary Completion Date
May 2015 (Anticipated)
Study Completion Date
August 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Institute of Respiratory Diseases, Mexico

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether extra fine formoterol/beclomethasona are more effective in the treatment of asthmatic crisis when added to conventional treatment compared with conventional treatment alone.
Detailed Description
Inhaled corticosteroids still the cornerstone in treatment of stable asthma, while bronchodilators and systemic steroids are in asthmatic crisis. Asthmatic exacerbations are events occurring in the natural course of the disease, require a change in actual medication and they are associated with risks of complications producing important economic costs. Some is known about non-genomic effects of inhaled corticosteroids, making possible, at least in theory, having a positive effect on treatment of a crisis. On the other hand, formoterol has been shown to have a rapid beginning of action (3 minutes), persisting its effect during 12 hours and it has been shown to be as effective as albuterol in the treatment of a crisis. The development of extra-fine particles has allowed reaching more distal zones in the lungs producing more deposition of the drug, which as well decrease adverse effects are lesser doses of the drug are needed. According to that, aims of this work is to determine whether extra-fine formoterol/beclomethasona are more effective in the treatment of asthmatic crisis when added to conventional treatment compared with conventional treatment in terms of pulmonary function, symptoms, inflammation markers and rates of hospitalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Asthmatic Crisis
Keywords
formoterol/beclomethasone in asthmatic crisis, asthmatic crisis treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Extra fine Formoterol/Beclomethasone
Arm Type
Active Comparator
Arm Description
Group receiving the drug additional to standard treatment standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline, 0, 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + formoterol/beclomethasone, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Group receiving placebo additional to standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline (0), 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + Placebo, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes
Intervention Type
Drug
Intervention Name(s)
Extra fine Formoterol/Beclomethasone
Other Intervention Name(s)
Innovair
Intervention Description
standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline (0), 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + formoterol/beclomethasone, 3 puffs administered via aerochamber at baseline (0), 20, 40, 60 minutes
Primary Outcome Measure Information:
Title
Pulmonary Function
Description
change in Forced Expiratory Volume in 1 second (FEV1) with respect to basal
Time Frame
120 minutes
Secondary Outcome Measure Information:
Title
Need for hospitalization
Time Frame
120 minutes
Title
Change in perception of dyspnea
Description
change in Borg and Transitional Dyspnea Index
Time Frame
90 minutes
Title
Biomarkers of inflammation
Description
change in C- reactive protein, TNF-alpha, eosinophils
Time Frame
120 minutes
Title
interleukins
Description
change in eosinophilic and non eosinophilic interleukins (IL-4, IL-5, IL-13, IL-17, IL-33)
Time Frame
120 min
Other Pre-specified Outcome Measures:
Title
Length of stay in hospital
Description
in patients requiring hospitalisation, evaluate length of stay
Time Frame
1 week
Title
adverse effects
Description
adverse effects related to the drug
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: previous asthma diagnosis by physician spirometry with quality grade A, B or C presenting with asthmatic crisis in emergency room Exclusion Criteria: imminent respiratory arrest respiratory comorbidities (COPD, cystic fibrosis, interstitial lung disease, pneumothorax, bronchiectasis) use of systemic steroids in 3 months previous allergy to steroids Peripheral capillary oxygen saturation (SpO2) less than 88%.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jose Luis Miguel, MD, MsC
Organizational Affiliation
National Institute of Respiratory Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institute of Respiratory Diseases
City
Mexico
State/Province
Distrito Federal
ZIP/Postal Code
14080
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
24041942
Citation
Martinez FD, Vercelli D. Asthma. Lancet. 2013 Oct 19;382(9901):1360-72. doi: 10.1016/S0140-6736(13)61536-6. Epub 2013 Sep 13.
Results Reference
background
PubMed Identifier
22832835
Citation
Garcia-Sancho C, Fernandez-Plata R, Martinez-Briseno D, Franco-Marina F, Perez-Padilla JR. [Adult asthma in Mexico City: a population-based study]. Salud Publica Mex. 2012 Jul-Aug;54(4):425-32. doi: 10.1590/s0036-36342012000400013. Spanish.
Results Reference
background
PubMed Identifier
15006973
Citation
Rodrigo GJ, Rodrigo C, Hall JB. Acute asthma in adults: a review. Chest. 2004 Mar;125(3):1081-102. doi: 10.1378/chest.125.3.1081.
Results Reference
background
PubMed Identifier
24899370
Citation
Lipworth B, Manoharan A, Anderson W. Unlocking the quiet zone: the small airway asthma phenotype. Lancet Respir Med. 2014 Jun;2(6):497-506. doi: 10.1016/S2213-2600(14)70103-1.
Results Reference
background

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Extra-fine Formoterol/Beclomethasone in Asthmatic Crisis

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