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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03849625
Other study ID # Chula-ARC 002/13
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2015
Est. completion date March 31, 2020

Study information

Verified date February 2022
Source Chulalongkorn University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Study clinical characteristics and phenotypes of patients diagnosed with NSAID sensitivity in Thailand


Recruitment information / eligibility

Status Completed
Enrollment 158
Est. completion date March 31, 2020
Est. primary completion date February 28, 2020
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion Criteria: - Thai patients with a history of an immediate reaction to aspirin/paracetamol, or NSAIDs visiting King Chulalongkorn memorial Hospital Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
aspirin, NSAIDs, paracetamol
Perform skin test and/or provocation test with aspirin, paracetmol, or suspected NSAIDs in questionable cases

Locations

Country Name City State
Thailand Faculty of Medicine, Chulalongkorn University Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Chulalongkorn University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Klaewsongkram J, Buranapraditkun S, Mongkolpathumrat P, Palapinyo S, Chantaphakul H. Clinical Characteristics, Urinary Leukotriene E4 Levels, and Aspirin Desensitization Results in Patients With NSAID-Induced Blended Reactions. Allergy Asthma Immunol Res. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Results of skin test/provocation test Positive, negative, or equivocal 4 years
Secondary Phenotypes of allergic reactions 4 years
Secondary Urine leukotriene E4 4 years
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