Effects of a High or Low Salycilate Diet on Urinary LTE4 and Clinical Features in AERD (AERD)
Primary Purpose
Aspirin-exacerbated Respiratory Disease, Aspirin-Sensitive Asthma With Nasal Polyps, Samter's Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Low salycilate diet
Sponsored by
About this trial
This is an interventional supportive care trial for Aspirin-exacerbated Respiratory Disease
Eligibility Criteria
Inclusion Criteria:
- Confirmed Aspirin exacerbated respiratory disease.
- Controled asthma
- No actual systemic corticosteroid treatment
- No antileucotriene treatment.
Exclusion Criteria:
- Patients who do not complete both phases of the study
- Patients unable to perform adecuate spyrometric testing
- Patients who present severe asthmatic reactions with high salycilate foods
Sites / Locations
- Instituto Nacional de Enfermedades Respiratorias
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Group 1
Group 2
Arm Description
Low salycilate diet on day one and High salycilate diet on day 7
High salycilate diet on day one and Low salycilate diet on day 7
Outcomes
Primary Outcome Measures
Change from baseline in Urinary concentration of Leucotriene E4 (LTE4)
pg/ml of creatinine
Secondary Outcome Measures
Change from baseline in Expiratory Volume in 1 second (FEV-1)
Percentage of referenced value
Change from baseline in Vital Capacity (FVC)
Percentage of referenced value
Change from baseline in the Relationship between FEV1/FVC
Percentage of referenced value
Change from baseline in the total nasal resistance obtained by rhinometry
pascals/cm3/sec
Full Information
NCT ID
NCT03973749
First Posted
February 6, 2019
Last Updated
June 3, 2019
Sponsor
Instituto Nacional de Enfermedades Respiratorias
1. Study Identification
Unique Protocol Identification Number
NCT03973749
Brief Title
Effects of a High or Low Salycilate Diet on Urinary LTE4 and Clinical Features in AERD
Acronym
AERD
Official Title
Effects of a High or Low Salycilate Diet on Urinary Leucotriene E4 Levels and Clinical Features in Patients With Aspirin Exacerbated Respiratory Disease
Study Type
Interventional
2. Study Status
Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 2, 2017 (Actual)
Primary Completion Date
May 31, 2019 (Anticipated)
Study Completion Date
May 31, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Nacional de Enfermedades Respiratorias
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
On day one, two groups of nine patients each will respectively recieve the tree daily meals (breakfast, Lunch and dinner) in a controled clinical setting. Group 1 will recieve a low-salycilate diet, and group 2 a high-salycilate diet. Two hours after each meal, urinary Leucotriene E4, FEV1, FVC, FEV1/FVC and total nasal resistance will be measured. On day 7, after clearance time, group 1 will recieve high-salycilate diet and group 2 low salycilate diet and the same measurements will be obtained.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aspirin-exacerbated Respiratory Disease, Aspirin-Sensitive Asthma With Nasal Polyps, Samter's Syndrome, Widal Syndrome
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group 1
Arm Type
Experimental
Arm Description
Low salycilate diet on day one and High salycilate diet on day 7
Arm Title
Group 2
Arm Type
Experimental
Arm Description
High salycilate diet on day one and Low salycilate diet on day 7
Intervention Type
Other
Intervention Name(s)
Low salycilate diet
Other Intervention Name(s)
High salycilate diet
Intervention Description
Each arm of the experimental group will be exposed to low and high concentrations of dietary salycilates and urinary LTE4, FEV1, FVC, FEV1/FVC and total inspiratory nasal resistance will be measured at basal level and then two hours after each of the 3 daily meals.
Primary Outcome Measure Information:
Title
Change from baseline in Urinary concentration of Leucotriene E4 (LTE4)
Description
pg/ml of creatinine
Time Frame
Baseline-4-8-12 hours in day one and Baseline-4-8-12 hours in day 7
Secondary Outcome Measure Information:
Title
Change from baseline in Expiratory Volume in 1 second (FEV-1)
Description
Percentage of referenced value
Time Frame
Baseline-4-8-12 hours and Baseline-4-8-12 hours in day 7
Title
Change from baseline in Vital Capacity (FVC)
Description
Percentage of referenced value
Time Frame
Baseline-4-8-12 hours and Baseline-4-8-12 hours in day 7
Title
Change from baseline in the Relationship between FEV1/FVC
Description
Percentage of referenced value
Time Frame
Baseline-4-8-12 hours and Baseline-4-8-12 hours in day 7
Title
Change from baseline in the total nasal resistance obtained by rhinometry
Description
pascals/cm3/sec
Time Frame
Baseline-4-8-12 hours and Baseline-4-8-12 hours in day 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Confirmed Aspirin exacerbated respiratory disease.
Controled asthma
No actual systemic corticosteroid treatment
No antileucotriene treatment.
Exclusion Criteria:
Patients who do not complete both phases of the study
Patients unable to perform adecuate spyrometric testing
Patients who present severe asthmatic reactions with high salycilate foods
Facility Information:
Facility Name
Instituto Nacional de Enfermedades Respiratorias
City
Mexico City
State/Province
Ciudad DE Mexico
ZIP/Postal Code
14080
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
No
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Effects of a High or Low Salycilate Diet on Urinary LTE4 and Clinical Features in AERD
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