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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02666092
Other study ID # 2013_43
Secondary ID 2014-A00855-42
Status Completed
Phase N/A
First received January 25, 2016
Last updated January 17, 2017
Start date February 2015
Est. completion date January 2017

Study information

Verified date January 2017
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anisakidae frequently infect fish species that are commonly eaten by humans. Some of them are recognized as zoonotic diseases agents, and have a high impact on human health.

Infestation results from the ingestion of living larvae from contaminated fishes. It can be asymptomatic or symptomatic, resulting in acute gastric, acute intestinal or chronic forms. Allergic manifestations are frequently encountered in gastric forms, but allergic symptoms can also occur in isolation, after ingestion of Anisakidae antigens contained in raw or cooked fish, and may masquerade as fish allergy.

In this study, we aim to characterize the relationship between Anisakidae and/or fish sensitization and the presence of allergic manifestations in patients recruited in the general population and presenting fish allergy resulting from ingestion, cutaneous or respiratory contact. We will also determine the respective role of Anisakidae or fish sensitization in patients with fish allergy. Then, we will determine the prevalence of previous Anisakidae infections among these patients and a matched control population. We will also compare the performances of serological tests (ImmunoCAP, immunoelectrophoresis and Western Blot) for the diagnosis of Anisakidae allergy or infection. Lastly, we will explore the relationship between domestic exposure to Anisakidae or fish antigens and the occurrence of associated pathologies (Anisakidae or fish allergy/sensitization; Anisakidae infection).


Description:

First, 51 patients with fish allergy will be recruited from the Parasitology-Mycology and Immunology Laboratories of Lille University Hospital databases (serology for anti-Anisakis or anti-fish detection). Then, clinical (characteristics of allergic manifestations) and epidemiological (domestic exposure to fish) data will be collected, and anti-fish or Anti-Anisakis antibodies will be detected using ImmunoCAP (IgE), or ImmunoCAP, immunoelectrophoresis, Western Blot, respectively. Similar serological tests will be performed for a control group of 51 matched subjects who will be recruited among Lille University Hospital workers.


Recruitment information / eligibility

Status Completed
Enrollment 105
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

ALLERGIC PATIENTS:

- Previous serological assessment for anti-Anisakis or anti-fish antibodies detection (ImmunoCap and/or immunoelectrophoresis) in Lille University Hospital Center, and volume of serum conserved =500 µl

- Allergic manifestations after contact with fish (asthma, allergic rhinitis, conjunctivitis, chronic or acute urticaria, dermatitis/eczema, eosinophilic gastroenteritis, gingivostomatitis, angioedema, bronchospasm, anaphylaxis)

CONTROL SUBJECTS:

- Serological assessment for infectious disease during a routine occupational health consultation in Lille University Hospital Center

- Absence of fish allergy

Exclusion Criteria:

- Pregnant or breast-feeding female

- Patient with no social insurance

- Patient unwilling to comply with the protocol

- Patient unable to understand the study and its objectives

- Patient under guardianship

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire
Questionnaire on domestic exposure to fish, and, for patients with fish allergy, on the characteristics of clinical manifestations)
Biological:
Detection of anti-Anisakis and anti-fish antibodies
Anti-fish IgE will be detected using ImmunoCAP. Anti-Anisakis antibodies will be detected using ImmunoCAP (IgE), immunoelectrophoresis (precipitins) and Western Blot.

Locations

Country Name City State
France CHRU Lille

Sponsors (5)

Lead Sponsor Collaborator
University Hospital, Lille ANSES, Boulogne-sur-Mer, Hôpital Cochin, Institut Pasteur de Lille, Région Nord-Pas de Calais, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the frequency of anti-Anisakis and/or anti-fish IgE by serum analysis comparison between subjects with fish allergy and a matched control population, presenting no fish allergy. contact by phone during 30 min at only visit (inclusion)
Secondary anti-Anisakis and/or anti-fish IgE level by serum analysis Comparison between subjects with fish allergy and a matched control population, presenting no fish allergy. contact by phone during 30 min at only visit (inclusion)
Secondary the frequency of anti-Anisakis and anti-fish IgE in patients with fish allergy by serum analysis contact by phone during 30 min at only visit (inclusion)
Secondary nomber of subjects of previous Anisakidae infections questionnaire-based diagnosis, supported by serological testing between patients with fish allergy and a matched control population, presenting no fish allergy. contact by phone during 30 min at only visit (inclusion)
Secondary Measure of the performances of serological tests Comparison of the performances of serological tests (ImmunoCAP, immunoelectrophoresis and Western Blot) for the diagnosis of Anisakidae allergy or infection. at work medical visit (inclusion)
Secondary The frequency of domestic exposure to fish parasites antigens by questionnaire It will be compared between Anisakis or fish allergic/sensitized subjects and non-allergic/non sensitized subjects.
It will be compared between patients with or without previous Anisakidosis. Fish exposure will be determined taking into account the handled fish species and the local prevalences of fish parasites.
contact by phone during 30 min at only visit (inclusion)
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