Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Controlling Aedes mosquitoes in Kinshasa

Official title: Implementation and Evaluation of Vector Control Methods in Kinshasa: The Case of Aedes, Vectors of Arboviruses.

Run by Institute of Tropical Medicine, Belgium · NCT06981442 · Data updated 2026-11-12

This study is testing different ways to control Aedes mosquitoes in Kinshasa to see if it helps reduce the spread of diseases like dengue and chikungunya.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment2050 (estimated)
SponsorInstitute of Tropical Medicine, Belgium
Academic / other
Locations1 site (Kinshasa, République Démocratique Du Congo)
StatusRecruiting
StartedMarch 26, 2025
Main results expectedSeptember 30, 2026
Study endsDecember 31, 2026
Registry record updatedAugust 19, 2026
Trial IDNCT06981442 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older who reside in selected health areas of Kinshasa and consent to participate.

Probably not a fit

Patients who are under 18 years of age, seriously ill, or not residing in the designated health zones may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to implement and evaluate various strategies for controlling Aedes mosquitoes, which are responsible for transmitting diseases like dengue and chikungunya, in Kinshasa, Democratic Republic of the Congo. It will utilize a before-and-after interventional approach to assess the effectiveness of community-based environmental management and targeted vector control methods at different life stages of the mosquitoes. Additionally, a serological survey will be conducted to gather data on the prevalence of Aedes-borne diseases in the area, enhancing understanding of their circulation.

Why it matters

Potential benefit: If successful, this study could significantly reduce the incidence of Aedes-borne diseases in the affected populations.

How similar studies have gone: Other studies have shown success with similar vector control approaches, indicating potential for effective interventions in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
At household level:

Inclusion Criteria:

* Belong to a household in one of the 4 health areas selected as study arms
* From 18 years of age to consent for household enrollment and participation in the serosurvey
* Consenting

Exclusion Criteria:

* Not belong to a household in one of the 4 health areas selected as study arms
* Under 18 years of age
* Non-consenting

At health facility level:

Inclusion Criteria:

* From 18 years of age
* Resident of the health zone of Mont Ngafula 1
* Consenting

Exclusion Criteria:

* Under 18 years of age
* Not resident in the health zone of Mont Ngafula 1
* Seriously ill and hospitalized, requiring transfusion, presence of blood clotting disorders, allergies resulting from injections, adverse events associated with previous blood sampling, pregnancy
* Non-consenting

Where it's running

  • Institut National de Recherche Biomédicale, INRB
    Kinshasa, République Démocratique Du Congo, Democratic Republic of the Congo
    Recruiting

Study contacts

  • Principal investigator: Veerle Vanlerberghe — Institute of Tropical Medicine Antwerp
  • Study coordinator: Luciana Lepore
  • Email: llepore@itg.be
  • Phone: +32(0)32476666

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.