- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06711861
Multicenter Retrospective Study on Streptobacillus Moniliformis Infections in France (Streptobacil)
November 28, 2024 updated by: University Hospital, Strasbourg, France
French data on Streptobacillus moniliformis infections (zoonosis transmitted by rat bites) are rare and there are no case series in the literature to date.
This is a pathology presenting atypical clinical manifestations for a bacterial infection and which therefore remains underdiagnosed.
Streptobacillus moniliformis infections can be fatal without appropriate antibiotic treatment.
This study could improve diagnosis, develop early treatment strategies and contribute to the overall understanding of zoonotic diseases
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
20
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: François DANION, MD
- Phone Number: 33 3 69 55 15 88
- Email: francois.danion@chru-strasbourg.fr
Study Locations
-
-
-
Strasbourg, France, 67091
- Recruiting
- Service des Maladies Infectieuses et Tropicales - CHU de Strasbourg - France
-
Contact:
- François DANION, MD
- Phone Number: 33 3 69 55 15 88
- Email: francois.danion@chru-strasbourg.fr
-
Principal Investigator:
- François DANION, MD
-
Sub-Investigator:
- Frédéric SCHRAMM, MD
-
Principal Investigator:
- Amandine ROBERT, MD
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Principal Investigator:
- GUILLOUZOUIC GUILLOUZOUIC, PharmD
-
-
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
No
Sampling Method
Non-Probability Sample
Study Population
Patient having Streptobacillus moniliformis infection between 01/01/2007 and 31/12/2023
Description
Inclusion Criteria:
- Minor patient aged 1 to 17 years
- Adult patient ≥18 years
- Proven Streptobacillus moniliformis infection between 01/01/2007 and 31/12/2023
- Subject not objecting, after being informed, to the reuse of their data for the purposes of this research
- Holders of parental authority not objecting, after being informed, to the reuse of their data for the purposes of this research their child for the purposes of this research
Exclusion Criteria:
- Subject and/or holder of parental authority having expressed opposition to participating in the study
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Retrospective study of the effectiveness of antibiotic therapy initiated for the treatment of Streptobacillus moniliformis infection.
Time Frame: Negative blood culture 15 days after the start of antibiotic therapy.
|
Clinical cure 15 days after the start of antibiotic therapy.
This cure is based on a negative blood culture (absence of germs) performed 15 days after the start of treatment.
|
Negative blood culture 15 days after the start of antibiotic therapy.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
February 16, 2024
Primary Completion (Estimated)
February 16, 2025
Study Completion (Estimated)
February 16, 2025
Study Registration Dates
First Submitted
August 21, 2024
First Submitted That Met QC Criteria
November 28, 2024
First Posted (Estimated)
December 2, 2024
Study Record Updates
Last Update Posted (Estimated)
December 2, 2024
Last Update Submitted That Met QC Criteria
November 28, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9237
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.