Response Rate to Ceftriaxone 1g IM in Gonorrhoea : a French Retrospective Monocentric Study
NCT ID: NCT04902560
Last Updated: 2021-10-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
120 participants
OBSERVATIONAL
2021-05-01
2021-08-01
Brief Summary
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Patients wanting STI screening can consult either they are symptomatic or not.
If they are symptomatic, they can be treated immediately. If they are not symptomatic, they must come back seven days after in order to get their results and to be treated if necessary.
Before any treatment for gonorrhea, subjects should be sampled for bacterial culture in order to perform AMR surveillance.
After every treatment for gonorrhea, subjects should realized a test of cure (TOC) according to current recommandation.
Response rate to ceftriaxone 1g IM for treating gonorrhea has never been evaluated in France while being used widely over the past months.
Compliance to current recommandation at CeGIDD Montpellier has never been evaluated.
This study will assess the response rate to ceftriaxone 1g IM as gonorrhea treatment by realizing a test of cure 14 days after each treatment.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Non-opposition form given to the subject
* Having at least one exam positive for Gonorrhoea (PCR or Culture), realised in CeGIDD de Montpellier
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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Du Thanh Aurelie
Role: STUDY_DIRECTOR
University Hospital, Montpellier
Locations
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Uhmontpellier
Montpellier, , France
Countries
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Other Identifiers
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RECHMPL21_0301
Identifier Type: -
Identifier Source: org_study_id