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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04902560
Other study ID # RECHMPL21_0301
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2021
Est. completion date August 1, 2021

Study information

Verified date October 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sexual health centers (CeGIDD, in France) manage the majority of STI in France, especially gonorrhea. 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.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date August 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Aged more than 18 years old - 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: - patient's refusal to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response rate to Ceftriaxone 1g IM in Gonorrhoea. Evaluated by a test of cure (TOC) which must be negative 15 days after the subject received the treatment (ceftriaxone). day 1
Secondary Adverse drug reaction rates Any adverse effect after treatment will be notified (digestive disorder, headache, phototoxicity, allergic reaction, local reaction at the site of injection…) day 1
Secondary Concordance rate with positive PCR Before getting the treatment, all patients should have been sampled for bacterial culture according to current recommendation. Respect of the recommendation will be assessed by this outcome. day 1
Secondary Resistance rate to ceftriaxone and AMR description. This measure will be assessed via bacterial cultures day 1
Secondary Rate of untreated patient despite having a positive test for gonorrhea (lost to follow-up) Patient compliance may be lacking in sexual health center and non-compliance participate in STI spreading.
Subject not looking for their results after being tested positive for gonorrhea will be notified by phone call. The necessity of calling the patient will be notified in the study.
If the subject does not attend the medical consultation for treatment, he will be consider as lost to follow-up.
day 1
Secondary Rate of realized TOC Test of cure (TOC) is a PCR test realized at the previous positive site of contamination, approximately 14 days after treatment, in order to confirm the efficacity of treatment. day 1
Secondary Rate of time before realizing the TOC. Sensibility and Specifity may differ depending on the time between treatment and the TOC. day 1
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