Actively Recruiting

Phase Not Applicable
All Genders
ID06894901

Assessing the Efficacy of Incompatible Insect Technique Coupled with Sterile Insect Technique (IIT-SIT) to Manage Large Dengue Clusters: a Randomized Controlled Trial

Led by National Environment Agency, Singapore · Updated on 2025-03-25

900

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

N

National Environment Agency, Singapore

Lead Sponsor

M

Ministry of Health, Singapore

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the use of Wolbachia-infected male mosquitoes combined with sterile insect technique (IIT-SIT) to reduce active dengue transmission in Singapore. This randomized controlled trial aims to determine if releasing these modified mosquitoes can limit the growth of dengue clusters, which are defined by two or more dengue cases occurring close in time and location. The study will provide evidence on whether IIT-SIT can be an effective additional tool for outbreak management in urban areas facing increasing dengue risks due to climate and urban changes. The trial involves randomly assigning dengue clusters in high-rise public housing estates to either receive the IIT-SIT intervention or serve as controls without mosquito releases. Clusters in the intervention group will have male Wolbachia-infected Aedes aegypti mosquitoes released continuously until no new dengue cases are linked to the cluster, while both groups will also receive the usual vector control measures from the National Environment Agency. This design closely mimics real-time outbreak management using IIT-SIT to assess its feasibility and challenges before wider use. Participants will be monitored for up to three years to assess outcomes such as the time until dengue cluster extinction and the final number of dengue cases in each cluster. Additional measurements include mosquito prevalence and dengue transmission risk. The study will track these indicators through laboratory-confirmed dengue cases and mosquito surveillance, providing detailed data on the intervention's impact on dengue spread and contributing to improved outbreak control strategies.

CONDITIONS

Brief Title

Impact of IIT-SIT on Dengue Clusters

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Dengue clusters must be in public housing estates
  • Clusters must have at least 10 reported dengue cases before assignment
  • The first 10 dengue cases must occur within 30 days of the first case
  • Clusters must be in areas with a sector-level GAI of at least 0.2 at the 10th reported case
  • Clusters must be in areas that have never had Wolbachia-Aedes mosquito releases
  • Clusters must be at least 700 meters away from existing Wolbachia-Aedes release areas
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 3 years

Participants in intervention clusters receive releases of male Wolbachia-infected Aedes aegypti mosquitoes until no further dengue cases are linked to the cluster. Participants in non-intervention clusters do not receive these releases but undergo usual outbreak management practices.

Ongoing monitoring visits during treatment period

Follow-up

Duration - Up to 3 years

Participants are monitored to assess the long-term impact of the intervention on dengue cluster extinction and size.

Periodic visits for up to 3 years

Trial Site Locations

Total: 1 location

1

National Environment Agency

Singapore, Singapore

Actively Recruiting

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Research Team

L

Lee Ching Ng, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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