Trial · NCT07884656
Optimizing Antibiotic Prescription in STI Clinics Using Rapid POCT
NCT07884656, Not applicable, Not yet recruiting, Hospices Civils de Lyon
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimizing Antibiotic Prescription in STI Clinics Using Rapid POCT. Trials, record NCT07884656. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07884656
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimizing Antibiotic Prescription in STI Clinics Using Rapid POCT
- NCT number
- NCT07884656
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 404 participants, estimated
- Lead sponsor
- Hospices Civils de Lyon
- Conditions
- Chlamydia Trachomatis Infection, Neisseria Gonorrhoeae Infection, Sexually Transmitted Infections, Antimicrobial Resistance / Antibiotic Overuse
- Interventions
- cobas® Liat® CT/NG Point-of-Care Test
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of antibiotic prescriptions avoided using POCT cobas® Liat® CT/NG | Day 0 (data collected at the inclusion consultation for each participant) | Percentage of participants for whom empirical or broad-spectrum antibiotic prescription was avoided due to immediate POCT results, compared with the theoretical standard-of-care prescribing strategy. |
| Secondary | Patient satisfaction score regarding POCT-based care | Day 0 (at the end of the consultation) | Patient-reported satisfaction measured using a standardized self-administered questionnaire immediately after consultation, evaluating comfort, understanding, and perceived usefulness of rapid testing. |
| Secondary | Healthcare Staff Satisfaction Index of integrating POCT into CeGIDD care pathways | Throughout study duration (12-month inclusion period) | staff satisfaction measured using a standardized self-administered French System Usability Scale (F-SUS) questionnaire |
| Secondary | Prevalence of non-target urogenital pathogens detected by standard culture | through study completion, an average of 1 year | Identification and proportion of other bacterial pathogens (e.g., Haemophilus spp.) isolated by routine culture in symptomatic participants, providing surveillance data complementary to POCT results. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07884656
GET https://conductscience.org/api/trials/v1/NCT07884656/registered