Gonorrhea Clinical Trial
— GONOCEFOfficial title:
Overall Patient Care in a Montpelier Sexual Health Center (CeGIDD). Response Rate to Ceftriaxone 1g IM in Gonorrhoea : a French Retrospective Monocentric Study
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 |
Verified date | October 2021 |
Source | University Hospital, Montpellier |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
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 |
Country | Name | City | State |
---|---|---|---|
France | Uhmontpellier | Montpellier |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Montpellier |
France,
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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