Clinical TrialID 3740
Effect of Dietary Salicylate in Aspirin Exacerbated Respiratory Disease
NCT01778465
Chronic Rhinosinusitis|Aspirin Exacerbated Respiratory Disease|Asthma|Aspirin Sensitivity
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 3740
- Evidence Id
- 3740
- Core Evidence Id
- 3740
- Source Clinical Trial Id
- 3713
- Herb2 Clinical Trial Id
- HBCT003713
- Nct Id
- NCT01778465
- Title
- Effect of Dietary Salicylate in Aspirin Exacerbated Respiratory Disease
- Status
- Completed
- Phase
- Study Result
- Yes
- Study Condition
- Chronic Rhinosinusitis|Aspirin Exacerbated Respiratory Disease|Asthma|Aspirin Sensitivity
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
- Intervention
- BEHAVIORAL: Low salicylate diet|BEHAVIORAL: Normal Diet
- Intervention Allocation
- Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 7
- Outcome Measure
- Urinary Levels of Cys-Leukotrienes, 14 days after commencement|Urinary Salicyluric Acid Levels, 14 days after commencement|Urinary Salicylic Acid Levels, 14 days after enrollment|Urinary Creatinine Levels, 14 days after commencement
- Sponsor Collaborator
- Lawson Health Research Institute
- Funded By
- OTHER
- Location
- St. Joseph's Health Care, London, Ontario, N5A 4V2, Canada
- Other Id
- 103330
- Start Date
- 2013-05
- Primary Completion Date
- 2014-03
- Completion Date
- 2014-05
- First Posted
- 2013-01-29
- Results First Posted
- 2021-03-09
- Last Update Posted
- 2021-03-09
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT01778465
- Title Cn
- Title En
- Effect of Dietary Salicylate in Aspirin Exacerbated Respiratory Disease
- Bilingual Status
- semi_complete