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Characteristics of Patients Diagnosed With NSAID Sensitivity in Thailand

Study Purpose

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

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Observational
Eligible Ages 15 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - Thai patients with a history of an immediate reaction to aspirin/paracetamol, or NSAIDs visiting King Chulalongkorn memorial Hospital.

Exclusion Criteria:

- None

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT03849625
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Chulalongkorn University
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Jettanong Klaewsongkram, MD
Principal Investigator Affiliation Chulalongkorn University
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries Thailand
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Aspirin Sensitivity, Aspirin-exacerbated Respiratory Disease, Aspirin-Induced Angioedema-Urticaria, Aspirin Allergy, NSAID-Induced Asthma, NSAID-Induced Angioedema-Urticaria, NSAID-Induced Anaphylactoid Reaction, Aspirin-Induced Anaphylactoid Reaction
Arms & Interventions

Arms

: NSAID sensitivity

Patients diagnosed with an immediate reaction to aspirin/NSAIDs/or paracetamol

Interventions

Drug: - aspirin, NSAIDs, paracetamol

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

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Bangkok, Thailand

Status

Recruiting

Address

Faculty of Medicine, Chulalongkorn University

Bangkok, , 10330

Site Contact

Jettanong Klaewsongkram, MD

Jettanong.K@chula.ac.th

662-2564152

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