TEST AND COMPARISON OF THE ALLERGINICITY OF DIFFERENT CARMIN-BASED PRODUCTS FOR POTENTIAL USE AS A COLORING ADDITIVE IN FOOD MANUFACTURING

Not Applicable

• Conditions: -L234 Allergic contact dermatitis due to dyes; Allergic contact dermatitis due to dyes; L234

• Registration Number: PER-062-09
• Lead Sponsor: CHR. HANSEN, A/S,

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2009-08-27
• Last Update Posted: 4 September 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 0

Inclusion Criteria

• Age between 20 and 60 years, both included
• People with pathophysiological problems compatible with respiratory allergy to cochineal-derived products, such as asthma or rhinoconjunctivitis, or at high risk of developing allergy to cochineal-derived products by exposure for several years. The same that will be obtained according to medical history.
• body mass index between 20 and 35 kg / m2, both values included.

Exclusion Criteria

• Subjects with diseases or immune system disorders such as autoimmune or immunosuppressive diseases for any cause, even if they are not receiving drug treatment for them at the present time.
• Subjects with relevant functional or structural abnormalities of the digestive system, such as malformations, angiodysplasia, active peptic ulcers or chronic inflammatory diseases.
• Subjects with any infectious pathology that requires antimicrobial treatment at the time of inclusion.
• Subjects who receive any type of treatment that modifies the immune response, such as immunosuppressants, corticosteroids, etc.
• Subjects with celiac disease.
• Subjects with debilitating pathologies such as diabetes and malignancies.
• Subjects with a poor state of hydration and nutrition.
• Subjects with important conditions in normal hematological and biochemical parameters.
• Subjects with obvious and documented current alcoholism.
• Subjects in which poor collaboration is foreseen or, in the opinion of the researcher, have difficulties to follow the development of the trial.
• Subject women who are pregnant or suspected of being pregnant.

Study & Design

• Study Type: Interventional
• Study Design: Not specified