- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01089465
Cimex Lectularius or Bed Bugs : Vector of Infectious Agents and Pathogenic Role
April 11, 2024 updated by: Centre Hospitalier Universitaire de Nice
During the last years, the investigators were the witness to the increase of a old emerging pest due to bed bugs (Cimex lectularius) in the world.
Insecticides resistances apparitions and internationals transports increases seem to be the reasons of the pest.
Cimex lectularius as vector of parasites, bacteria or virus was often suggested although not much observation are recently investigated in France.
This study intends to examine the vectorial ability and the direct pathogenicity of Cimex lectularius.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
135
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Pascal Delaunay, PH
- Phone Number: 04.92.03.62.54
- Email: delaunay.p@chu-nice.fr
Study Locations
-
-
-
Nice, France, 06000
- Collection of the bedbugs and dermatological follow-up of the stings
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- On the site of takings presence of insects and eggs evoking bedbugs of beds. The identification of certainty will be made in the laboratory. All the insects not apartment to the family of Cimicidae (Criterion of exclusion) are thrown(cast) in trash cans of laboratories for organic products.
- voluntary Patients after reading of the information sheet and the signature of the consent
- Membership of the patient in the national insurance scheme
Exclusion Criteria
- On the site of takings absence of insects and eggs evoking bedbugs of beds
- During the identification of certainty in the laboratory, the captured insects do not make parties of the family of Cimicidae
- The subjects deprived of freedom.
- Patients cancelling their consent.
- Patients violating the protocol of search(research)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Morphological identification of every bedbug Porterage of bacterial agents Porterage of viral agents Biomolecular identification of the insect A breeding of bedbugs Tests of sensibility in insecticides
Time Frame: day 1
|
day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Study of the direct pathogenicity of lectularius C.
Time Frame: day 1, 7, 15 and 30
|
During each of four consultations a questionnaire and a descriptive index card(form) of the general and dermatological signs will be informed.
The criteria of evaluation, associated with anonimisées photos, are split into two groups: general Signs and dermatological Signs
|
day 1, 7, 15 and 30
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Pascal Delaunay, Dr, Centre Hospitalier Universitaire de Nice
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2010
Primary Completion (Actual)
March 1, 2012
Study Completion (Actual)
December 31, 2019
Study Registration Dates
First Submitted
March 12, 2010
First Submitted That Met QC Criteria
March 17, 2010
First Posted (Estimated)
March 18, 2010
Study Record Updates
Last Update Posted (Actual)
April 12, 2024
Last Update Submitted That Met QC Criteria
April 11, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09-API-01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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