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Enrolling by invitationNCT06689397EBV ConjUpdated Nov 14, 2024

Investigating Epstein-Barr Virus Associated Conjunctivitis

An observational study in Conjunctivitis and EBV Infection, sponsored by Moorfields Eye Hospital NHS Foundation Trust. Enrolling by invitation at 1 site in United Kingdom. Open to participants aged 16 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-14.

Sponsored by Moorfields Eye Hospital NHS Foundation Trust · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 5 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
5
Ages
16 Years and older
Sex
All
01

Study summary

Conjunctivitis means inflammation of the conjunctiva, the thin transparent layer over the white of the eye and under the eyelids. Acute conjunctivitis caused by infection is the most common condition seen in ophthalmic emergency departments, accounting for up to 10% of cases. It is responsible for 41% of eye-related general practice consultations. A diagnosis is usually made on the patient's symptoms and signs, despite this being less reliable than laboratory testing. When a cause is found, it is usually a common cold virus called adenovirus, that gets better with time and does not require treatment.

Through investigating cases of conjunctivitis at Moorfields, it has been discovered that in addition to adenovirus, Epstein Barr virus (EBV) is sometimes detected in conjunctival swabs from individuals with conjunctivitis. EBV is a very common viral infection that 95% of adults have experienced. EBV infection mostly passes unnoticed but when symptoms do occur, they include a sore throat, high temperature, swollen glands and tiredness, often called glandular fever or infectious mononucleosis. Conjunctivitis can also occur. EBV remains in the body after infection and rarely causes further problems. The virus can become active again occasionally, which is known as reactivation.

Reactivation usually passes unnoticed but sometimes is associated with recurrence of symptoms. It is possible that reactivation may cause conjunctivitis. It is not certain, which is will be observed as a part of this study, as it might be the cause of some of the conjunctivitis seen.

Through a collaboration with University College London (UCL), the aim is to gain further insight into infectious conjunctivitis, particularly in relation to EBV. This will be done by taking a swab of the conjunctiva, a single blood test and a tiny (1-2mm) tissue sample from the inner eyelid. Improved knowledge will allow the research team to develop better guidance and treatment for patients with conjunctivitis.

02

Conditions studied

  • Conjunctivitis
  • EBV Infection
03

In context

Conjunctivitis

85 studies on the registry are indexed under Conjunctivitis; 5 are open to participants now.

This study's planned enrollment of 5 is below the median of 254 across 18 observational studies indexed under Conjunctivitis.

Browse Conjunctivitis studies →

Lead sponsor

Moorfields Eye Hospital NHS Foundation Trust is the lead sponsor of 48 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will be recruited from Moorfields A\&E. Eligible patients will be identified by a member of the clinical triage team. All eligible patients will be enrolled during the study period.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Participants shall be considered eligible for inclusion if:

    • Aged ≥16 years;
    • working diagnosis of infective (viral) follicular conjunctivitis (\<4 weeks duration)
    • EBV positive conjunctival swab

Exclusion criteria

Exclusion Criteria:

    • Present with symptoms/signs such that another diagnosis is deemed more likely, for example topical medication-induced conjunctivitis.

      • Participant declines diagnostic tests or appropriate corneal or conjunctival sample(s) not obtained for any reason
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
5 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. The number of participants with clinically suspected viral conjunctivitis in which EBV DNA is identified on NAAT.

    To confirm the proportion of: * participants with clinically suspected viral conjunctivitis in which EBV DNA is identified on NAAT. * EBV NAAT-positive participants who have a new EBV infection versus those with a reactivation of earlier disease. * participants in whom EBV is confirmed the cause of conjunctivitis on further investigation.

    Time frame: From enrollment to the end of visit 2 which can occur within up to 7 days from enrollment.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2024 (actual). Primary completion is estimated for Jun 2025, 7 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 8, 2024
First posted
Nov 14, 2024
StartActual
Oct 9, 2024
Primary completionEst.
Jun 2, 2025
CompletionEst.
Jun 2, 2025
Last update
Nov 14, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 14, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06689397
Lead sponsor
Moorfields Eye Hospital NHS Foundation Trust
Responsible party
Sponsor
First posted
Nov 14, 2024
Start date
Oct 9, 2024
Primary completion
Jun 2, 2025 (estimated)
Completion
Jun 2, 2025 (estimated)
Last update
Nov 14, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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