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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05313126
Other study ID # 2020-A03558-31
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 9, 2021
Est. completion date June 2023

Study information

Verified date March 2022
Source Institut de Recherche pour le Developpement
Contact Franck Remoué, PhD
Phone +33 (0)4 67 41 61 30
Email franck.remoue@ird.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is based on 2 complementary components, named ExpAlbo Biomarker and CAPAlbo Questionnaire 1. ExpAlbo Biomarker (Exposure to the Aedes albopictus mosquito): This component concerns the epidemiological evaluation of the effectiveness of the release of sterile male mosquitoes on the level of exposure of individuals to the bites of the tiger mosquito through the use of a new immunological biomarker of the human-vector contact, developed over the past 20 years by the IRD-MIVEGEC team. Indeed, when a person is bitten by a mosquito, he or she develops a defence reaction, called an immune reaction, against the mosquito's saliva. The main objective of this study is to measure this immune response, and more specifically the antibody response specifically directed against compounds (peptide = small fragment of a protein) in mosquito saliva, and to determine whether this anti-saliva antibody response, and therefore exposure to mosquito bites, decreases when the mosquito control strategy is applied. 2. CAPAlbo Questionnaire: This component is concerned with assessing the impact of sterile male mosquito releases on perceptions and practices related to exposure to Aedes albopictus based on population-based questionnaire surveys. The main objective of these surveys is to determine whether changes in objective exposure to Aedes albopictus mosquitoes are associated with changes in the perception of the nuisance and in the lifestyle habits of respondents, particularly those related to the prevention of mosquito bites (such as the use of repellents or mosquito nets).


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date June 2023
Est. primary completion date June 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - To inhabit on a regular basis in the intervention/control area - To speak French

Study Design


Related Conditions & MeSH terms


Intervention

Other:
sterile insect technique (TIS)
Sterile male Aedes albopictus mosquitos are released in the area/neighborhood

Locations

Country Name City State
France population générale (quartier Duparc (Sainte Marie) et Quartier Bois rouge) La Réunion

Sponsors (1)

Lead Sponsor Collaborator
Institut de Recherche pour le Developpement

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Immunological indicators Biomarker based on the measurement of human IgG antibody levels specific to one peptide of Aedes saliva (i.e. Nterm-24kDa salivary peptide) 6 months
Primary Immunological indicators Biomarker based on the measurement of human IgG antibody levels specific to one peptide of Aedes saliva (i.e. Nterm-24kDa salivary peptide) 12 months
Primary Exposure to Aedes mosquito self-perceived exposure to mosquito will be assessed by questionnaire 6 months
Primary Exposure to Aedes mosquito self-perceived exposure to mosquito will be assessed by questionnaire 12 months
Secondary Protective behavior a composite indicator derived from a questionnaire will rate the protective behavior of the participants to avoid mosquito bites 6 months
Secondary Protective behavior a composite indicator derived from a questionnaire will rate the protective behavior of the participants to avoid mosquito bites 12 months
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