GonorrheaNCT07671014
Metagenomic Analysis of the Pharynx in High Risk Partners
An observational study of Gonorrhea and Neisseria Gonorrhea, run by Guy's and St Thomas' NHS Foundation Trust.
Trial summary
The Neisseria gonorrhoea (NG) epidemic in England is at the highest level in one hundred years of public health records. The World Health Organisation has listed NG as one of the top five bacterial infections globally because of the ability of the bacteria to develop resistance to antibiotics. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Gonorrhea, Neisseria Gonorrhea, Neisseria Meningitidis
- How many people
- 100 participants
- Where
- No sites listed yet
- Study dates
- 14 Jul 2026to 28 Feb 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Most of the partners will be men who have sex with men as 80% of the diagnoses of gonorrhea are made in this group
Who may be able to join
- Partner alerted of their risk about being a partner of someone diagnosed with Neisseria Gonorrhea using the digital partner notification software SXT and then booking an appointment for standard of care testing.
Who cannot join
- Under 18 years, unable to speak English
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
Anatole S Menon-Johansson, BSc, PhD, MB, BChir, MPH, MBA contact
About this study
Official title: A Preliminary Investigation to Determine the Utility of Using Metagenomic Analysis of Pharyngeal Samples Taken From Partners of Patients Diagnosed With Gonorrhoea to Identify Organisms, Antibiotics Resistance and Virulence Factors of Neisseria Species and the Impact of STI Prevention Strategies (4CMenB Vaccination and DoxyPEP)
The Neisseria gonorrhoea (NG) epidemic in England is at the highest level in one hundred years of public health records. The World Health Organisation has listed NG as one of the top five bacterial infections globally because of the ability of the bacteria to develop resistance to antibiotics. Neisseria meningitidis (NM) is a common pharyngeal commensal and it has been shown to be in one in five men who have sex with men (MSM) in London.
In the last year sexual health clinics have had a growing number of MSM presenting with urethritis / proctitis that were treated for NG on the day only to be found later to have been infected with NM from the culture. It appear that virulence factors have been passed from NG to NM enabling these bacteria to infect the urogenital and anal mucosa; consequently, NM in some cases is a new Sexually Transmitted Infection (STI). In 2025, two STI prevention interventions were rolled out in an attempt to address the gonorrhoea \& syphilis epidemics and these were the 4CMenB vaccine and doxycycline post exposure prophylaxis (DoxyPEP).
Read more
This study will recruit sexual partners of patients who have been diagnosed with NG and the investigators will ask the participant for one additional pharyngeal sample for research that will not impact on their standard of care. The additional sample will be tested using metagenomics, that is where all non-human DNA is analysed, and the initial focus will be on NG or NM infection, co-infection, genes for virulence and antibiotic resistance from whole genome sequencing.
The metagenomic analysis is being undertaken for research purpose only; however, secondary outcomes will look for other STIs in the pharyngeal sample and sample turn around time to inform the management of patients. Any additional STI identified will have validated testing to confirm diagnosis.
Read the detailed description
The main focus of this study is to develop a metagenomic assay for sexually transmitted infections (STIs) using samples taken from the pharynx of sexual partners of a patient who has been diagnosed with gonorrhoea.
Initial analysis will be on the Neisseria species (N. gonorrhoea [NG] \& N.meningitidis [NM]) identified, co-infection, the virulence factors seen and mutations related to antibiotic resistance.
A full clinical history will be taken for each participant and the investigators will ask if they have had the 4CMenB vaccination (against NM with up to 30-40% protection against NG) or taken DoxyPEP (doxycycline 200mg taken after sex) because about 15% of NG is sensitive to tetracyclines.
The secondary research questions will focus on which other STIs are detectable using metagenomics in the pharynx. It is possible that there will be co-infections with Chlamydia trachomatis (serovars D-K and L1-3), Mycoplasma genitalium, Treponema pallidum, Human Papillomavirus and Herpes viruses.
The study will also explore the feasibility, turnaround times, and potential operational considerations associated with metagenomic sequencing within a sexual health research setting.
The metagenomic assay is being used for research purposes only and is not being used as a validated diagnostic test to direct participant management.
Current testing for gonorrhoea (NG) involves a targeted test which uses a primer (a genetic key which is different for each infection) and then the amplification of the Deoxyribonucleic Acid (DNA) or RiboNucleic Acid (RNA).
The clinical team only see what they test for; consequently, if they don't order an NG test then it will be missed. In addition, there is no targeted test for Neisseria meningitidis (NM) in sexual health; therefore, clinical teams only 'see' this infection if the laboratory are able to grow the organism in culture. Culture for NG is only positive in 50% of cases with the standard of care pathway. When an organism does not grow then it is not possible to do antibiotic sensitivity testing.
Metagenomic testing enables the laboratory to identify what organisms are present and then do additional analysis to understand what treatments would be expected to work. The investigators can also use whole genome sequencing to investigate the exchange of genetic material from NG to NM to understand what is driving the change in the clinical presentation.
Testing in London has shown that one in five men who have sex with men (MSM) carry NM in their throat. The current epidemic of NG is unprecedented and the strategy of frequent testing has not helped stem this rise. The recent recommendation to give high risk MSM the 4CMenB vaccine (against NM) has been done with the hope of producing cross protection to NG too. Some studies have shown a 30-40% reduction in NG so it will be interesting to see how that impacts the positivity in partners. Historically 45% of sexual partners of patients diagnosed with NG are found to have the infection.
The roll out of doxycycline as post exposure prophylaxis (DoxyPEP) to reduce the risk of syphilis by 80% will also partially impact on GC too as 15% of these bacteria are still sensitive to this group of antibiotics (tetracyclines).
The identification of gyrA mutation in NG means that it will be resistant to quinolone treatment; however, if it is not present then these patients could be treated with a single ciprofloxacin tablet from pharmacy instead of coming back to clinic for an intramuscular injection with the third generation cephalosporin, Ceftriaxone. In London, half of the NG are still sensitive to quinolones; consequently, identifying that this treatment could be used would speed up access to treatment and release capacity in clinic.
Finally, the identification of other known sexually transmitted infections (STI) will be possible using metagenomics. Oral sex is already known to transmit Chlamydia, Syphilis and Herpes; therefore, this type of testing will enable the identification of infections that would traditionally be missed. During this trial the investigators will determine how metagenomic testing could fit in with the standard of care pathways to support optimal STI control.
In this study the investigators are going to focus on the sexual partners of patients who have been diagnosed with Neisseria gonorrhoea (NG). The rationale for this choice is because data from the UK HSA shows that 45% of these partners will have the infection; consequently, sampling this group will enable us to have nearly a 1:1 ratio of individuals with an NG infected pharynx and a control. One in five will be expected to have Neisseria Meningitidis (NM).
Partners will be alerted of their risk using the anonymous partner notification platform SXT (http://sxt.health) and attracted to the Burrell Street Sexual Health clinic through the provision of targeted appointments. The SXT software shows local appropriate clinics for partners to access testing, treatment and other STI prevention services and those clinics with appointments are prioritised on the clinic search.
When the partner is seen they will receive the normal standard of care which includes chlamydia/gonorrhoea testing from the pharynx, rectum and urine as well as culture testing from the three sites if they are going to be treated with an antibiotic. All eligible partners are offered the opportunity to join the study. If the partner consents to become a participant then add additional swab will be taken from the pharynx in addition to the standard of care. Partners (participants if they consent) who are asymptomatic and not had sex for two weeks will be offered tests only and to await the results.
This observational trial involves taking one additional swab from the pharynx for metagenomic analysis. Initially theses tests will be collected for batch testing and analysis. Later in the trial the investigators will work on the throughput of samples to determine if they can be used to inform the standard of care. If NG is detected then the investigators will determine that there is no quinolone resistance then this may alter treatment options in the future. During this study, metagenomic results will not be used to direct participant treatment or replace standard of care testing pathways.
All treatment decisions will continue to be based on validated standard clinical testing. While identification of quinolone-sensitive NG may inform future clinical investigation into alternative treatment pathways, including use of oral ciprofloxacin, this will not form part of participant management within the current study.
Other aspects of standard of care include blood testing for HIV, Syphilis, Hepatitis (A/B/C) as well as the offer of STI prevention services such as PrEP to reduce their risk of HIV, Vaccinations for Hepatitis A\&B, HPV, MPox and 4CMenB (against NM and NG) and DoxyPEP to reduce their risk of syphilis.
- Conditions
- Gonorrhea, Neisseria Gonorrhea, Neisseria Meningitidis, Metagenomic Next Generation Sequencing
- Keywords
- Gonorrhea, Metagenomic testing, Neisseria Gonorrhoea, Neisseria Meningitis
- Medical subject headings
- Gonorrhea, Meningitis, Meningococcal
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Sexual partner of someone diagnosed with Neisseria Gonorrhea infection | Partner alerted of their risk anonymous using SXT (http://sxt.health) and then these individuals booking an appointment to be seen for standard of care testing. If they are 18 years of age or older and can speak English then they will be offered the opportunity to join our observational study. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Neisseria species
Number of partners with Neisseria Gonorrhea or Neisseria Meningitidis infection identified in the pharynx, the presence of virulence factors and antibiotic resistance genes.
Measured: Within the week of sampling
Secondary outcomes (1)
Other sexually transmitted infections
We will be able to identify if other sexually transmitted infections are present in the pharynx. Possible additional organisms include: Treponema pallidum, Chlamydia trachomatis, Mycoplasma genitalium, human herpes virus 1/2, Human Papillomavirus
Measured: Within one week of sample being taken
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jun 2026
- Study start14 Jul 2026 (estimated)
- Primary completion31 Dec 2026 (estimated)
- Study completion28 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for GonorrheaStudies of the same condition, open and under way.
- More trials run by Guy's and St Thomas' NHS Foundation TrustThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Guy's and St Thomas' NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07671014
- Sponsor's protocol ID
- IRAS 368188
- Status last verified
- Jun 2026
- First submitted
- 22 Jun 2026
- Last updated
- 30 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: No patient identifiable data will be shared. We plan to do the metagenomic analysis alongside the standard of care and then look at the additional diagnostic information from this approach and determine if it adds value to our patients.
Publications
Alcolea-Medina A, Snell LB, Humayun G, Al-Yaakoubi N, Ward D, Alder C, Patel V, Vivian F, Meadows CIS, Wyncoll D, Paul R, Barratt N, Batra R, Edgeworth J, Nebbia G, Whitehorn J. Rapid pan-microbial metagenomics for pathogen detection and personalised therapy in the intensive care unit: a single-centre prospective observational study. Lancet Microbe. 2025 Oct;6(10):101174. doi: 10.1016/j.lanmic.2025.101174. Epub 2025 Oct 1.
PubMed 41045941
Study at a glance
From the registry record, last updated by the sponsor on 30 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Preliminary Investigation to Determine the Utility of Using Metagenomic Analysis of Pharyngeal Samples Taken From Partners of Patients Diagnosed With Gonorrhoea to Identify Organisms, Antibiotics Resistance and Virulence Factors of Neisseria Species and the Impact of STI Prevention Strategies (4CMenB Vaccination and DoxyPEP)
- ClinicalTrials.gov ID
- NCT07671014
- Acronym / sponsor ID
- IRAS 368188
- Conditions
- Gonorrhea, Neisseria Gonorrhea, Neisseria Meningitidis, Metagenomic Next Generation Sequencing
- Keywords
- Gonorrhea, Metagenomic testing, Neisseria Gonorrhoea, Neisseria Meningitis
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Guy's and St Thomas' NHS Foundation TrustUniversity, hospital or other
- Study start
- 14 Jul 2026 (estimated)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 28 Feb 2027 (estimated)
- First posted
- 26 Jun 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Neisseria gonorrhoea (NG) epidemic in England is at the highest level in one hundred years of public health records. The World Health Organisation has listed NG as one of the top five bacterial infections globally because of the ability of the bacteria to develop resistance to antibiotics. Neisseria meningitidis (NM) is a common pharyngeal commensal and it has been shown to be in one in five men who have sex with men (MSM) in London.
In the last year sexual health clinics have had a growing number of MSM presenting with urethritis / proctitis that were treated for NG on the day only to be found later to have been infected with NM from the culture. It appear that virulence factors have been passed from NG to NM enabling these bacteria to infect the urogenital and anal mucosa; consequently, NM in some cases is a new Sexually Transmitted Infection (STI). In 2025, two STI prevention interventions were rolled out in an attempt to address the gonorrhoea \& syphilis epidemics and these were the 4CMenB vaccine and doxycycline post exposure prophylaxis (DoxyPEP).
This study will recruit sexual partners of patients who have been diagnosed with NG and the investigators will ask the participant for one additional pharyngeal sample for research that will not impact on their standard of care. The additional sample will be tested using metagenomics, that is where all non-human DNA is analysed, and the initial focus will be on NG or NM infection, co-infection, genes for virulence and antibiotic resistance from whole genome sequencing.
The metagenomic analysis is being undertaken for research purpose only; however, secondary outcomes will look for other STIs in the pharyngeal sample and sample turn around time to inform the management of patients. Any additional STI identified will have validated testing to confirm diagnosis.
Detailed description
The main focus of this study is to develop a metagenomic assay for sexually transmitted infections (STIs) using samples taken from the pharynx of sexual partners of a patient who has been diagnosed with gonorrhoea.
Initial analysis will be on the Neisseria species (N. gonorrhoea [NG] \& N.meningitidis [NM]) identified, co-infection, the virulence factors seen and mutations related to antibiotic resistance.
A full clinical history will be taken for each participant and the investigators will ask if they have had the 4CMenB vaccination (against NM with up to 30-40% protection against NG) or taken DoxyPEP (doxycycline 200mg taken after sex) because about 15% of NG is sensitive to tetracyclines.
The secondary research questions will focus on which other STIs are detectable using metagenomics in the pharynx. It is possible that there will be co-infections with Chlamydia trachomatis (serovars D-K and L1-3), Mycoplasma genitalium, Treponema pallidum, Human Papillomavirus and Herpes viruses.
The study will also explore the feasibility, turnaround times, and potential operational considerations associated with metagenomic sequencing within a sexual health research setting.
The metagenomic assay is being used for research purposes only and is not being used as a validated diagnostic test to direct participant management.
Current testing for gonorrhoea (NG) involves a targeted test which uses a primer (a genetic key which is different for each infection) and then the amplification of the Deoxyribonucleic Acid (DNA) or RiboNucleic Acid (RNA).
The clinical team only see what they test for; consequently, if they don't order an NG test then it will be missed. In addition, there is no targeted test for Neisseria meningitidis (NM) in sexual health; therefore, clinical teams only 'see' this infection if the laboratory are able to grow the organism in culture. Culture for NG is only positive in 50% of cases with the standard of care pathway. When an organism does not grow then it is not possible to do antibiotic sensitivity testing.
Metagenomic testing enables the laboratory to identify what organisms are present and then do additional analysis to understand what treatments would be expected to work. The investigators can also use whole genome sequencing to investigate the exchange of genetic material from NG to NM to understand what is driving the change in the clinical presentation.
Testing in London has shown that one in five men who have sex with men (MSM) carry NM in their throat. The current epidemic of NG is unprecedented and the strategy of frequent testing has not helped stem this rise. The recent recommendation to give high risk MSM the 4CMenB vaccine (against NM) has been done with the hope of producing cross protection to NG too. Some studies have shown a 30-40% reduction in NG so it will be interesting to see how that impacts the positivity in partners. Historically 45% of sexual partners of patients diagnosed with NG are found to have the infection.
The roll out of doxycycline as post exposure prophylaxis (DoxyPEP) to reduce the risk of syphilis by 80% will also partially impact on GC too as 15% of these bacteria are still sensitive to this group of antibiotics (tetracyclines).
The identification of gyrA mutation in NG means that it will be resistant to quinolone treatment; however, if it is not present then these patients could be treated with a single ciprofloxacin tablet from pharmacy instead of coming back to clinic for an intramuscular injection with the third generation cephalosporin, Ceftriaxone. In London, half of the NG are still sensitive to quinolones; consequently, identifying that this treatment could be used would speed up access to treatment and release capacity in clinic.
Finally, the identification of other known sexually transmitted infections (STI) will be possible using metagenomics. Oral sex is already known to transmit Chlamydia, Syphilis and Herpes; therefore, this type of testing will enable the identification of infections that would traditionally be missed. During this trial the investigators will determine how metagenomic testing could fit in with the standard of care pathways to support optimal STI control.
In this study the investigators are going to focus on the sexual partners of patients who have been diagnosed with Neisseria gonorrhoea (NG). The rationale for this choice is because data from the UK HSA shows that 45% of these partners will have the infection; consequently, sampling this group will enable us to have nearly a 1:1 ratio of individuals with an NG infected pharynx and a control. One in five will be expected to have Neisseria Meningitidis (NM).
Partners will be alerted of their risk using the anonymous partner notification platform SXT (http://sxt.health) and attracted to the Burrell Street Sexual Health clinic through the provision of targeted appointments. The SXT software shows local appropriate clinics for partners to access testing, treatment and other STI prevention services and those clinics with appointments are prioritised on the clinic search.
When the partner is seen they will receive the normal standard of care which includes chlamydia/gonorrhoea testing from the pharynx, rectum and urine as well as culture testing from the three sites if they are going to be treated with an antibiotic. All eligible partners are offered the opportunity to join the study. If the partner consents to become a participant then add additional swab will be taken from the pharynx in addition to the standard of care. Partners (participants if they consent) who are asymptomatic and not had sex for two weeks will be offered tests only and to await the results.
This observational trial involves taking one additional swab from the pharynx for metagenomic analysis. Initially theses tests will be collected for batch testing and analysis. Later in the trial the investigators will work on the throughput of samples to determine if they can be used to inform the standard of care. If NG is detected then the investigators will determine that there is no quinolone resistance then this may alter treatment options in the future. During this study, metagenomic results will not be used to direct participant treatment or replace standard of care testing pathways.
All treatment decisions will continue to be based on validated standard clinical testing. While identification of quinolone-sensitive NG may inform future clinical investigation into alternative treatment pathways, including use of oral ciprofloxacin, this will not form part of participant management within the current study.
Other aspects of standard of care include blood testing for HIV, Syphilis, Hepatitis (A/B/C) as well as the offer of STI prevention services such as PrEP to reduce their risk of HIV, Vaccinations for Hepatitis A\&B, HPV, MPox and 4CMenB (against NM and NG) and DoxyPEP to reduce their risk of syphilis.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Sexual partner of someone diagnosed with Neisseria Gonorrhea infection | – | –Partner alerted of their risk anonymous using SXT (http://sxt.health) and then these individuals booking an appointment to be seen for standard of care testing. If they are 18 years of age or older and can speak English then they will be offered the opportunity to join our observational study. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Most of the partners will be men who have sex with men as 80% of the diagnoses of gonorrhea are made in this group
Key inclusion criteria (1 listed)
- Partner alerted of their risk about being a partner of someone diagnosed with Neisseria Gonorrhea using the digital partner notification software SXT and then booking an appointment for standard of care testing.
Key exclusion criteria (1 listed)
- Under 18 years, unable to speak English
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Neisseria species
Time frame: Within the week of sampling
Number of partners with Neisseria Gonorrhea or Neisseria Meningitidis infection identified in the pharynx, the presence of virulence factors and antibiotic resistance genes.
1 secondary outcome
Other sexually transmitted infections
Time frame: Within one week of sample being taken
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jun 2026.
- Results publication: PubMed 41045941Alcolea-Medina A, Snell LB, Humayun G, Al-Yaakoubi N, Ward D, Alder C, Patel V, Vivian F, Meadows CIS, Wyncoll D, Paul R, Barratt N, Batra R, Edgeworth J, Nebbia G, Whitehorn J. Rapid pan-microbial metagenomics for pathogen detection and personalised therapy in the intensive care unit: a single-centre prospective observational study. Lancet Microbe. 2025 Oct;6(10):101174. doi: 10.1016/j.lanmic.2025.101174. Epub 2025 Oct 1.
- Individual participant dataSharing planned: Yes. No patient identifiable data will be shared. We plan to do the metagenomic analysis alongside the standard of care and then look at the additional diagnostic information from this approach and determine if it adds value to our patients.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Anatole S Menon-Johansson, BSc, PhD, MB, BChir, MPH, MBA contact
Questions about this trial
What is this clinical trial studying?
An observational study of Gonorrhea and Neisseria Gonorrhea, run by Guy's and St Thomas' NHS Foundation Trust.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 30 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Anatole S Menon-Johansson, BSc, PhD, MB, BChir, MPH, MBA (+447900212512, a.menon-johansson@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Neisseria species (time frame: Within the week of sampling). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07671014, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jun 2026.