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Clinical Trials/NCT02490254
NCT02490254
Completed
Not Applicable

Childhood Uveitis Not Associated With Juvenile Idiopathic Arthritis: Incidence, Initial Management and One-year Outcomes

Moorfields Eye Hospital NHS Foundation Trust1 site in 1 country500 target enrollmentNovember 1, 2014
ConditionsUveitis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Uveitis
Sponsor
Moorfields Eye Hospital NHS Foundation Trust
Enrollment
500
Locations
1
Primary Endpoint
The primary outcome measure will be the total number of reported cases of uveitis.
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The investigators wish to establish a robust estimate of the incidence of inflammation inside the eye (uveitis) in children age 0-16 years in the UK, which hospitals children present to, where they are referred to, which treatment they receive during the first year after diagnosis, and how well they can see at the end of the first year.

Detailed Description

The investigators therefore propose to run a high quality surveillance study, together with the British Ophthalmological Surveillance Unit (BOSU) at the Royal College of Ophthalmologists and with the Scottish Ophthalmological Surveillance Unit (SOSU). BOSU and SOSU operate a monthly reporting card scheme. All UK consultant ophthalmologists and associate specialists receive a monthly 'report card' with a list of conditions being surveyed. Reporting clinicians will tick a box if they have seen a case of childhood uveitis in the preceding month, and return the card to BOSU/SOSU, who will inform us, the study investigators. Following reporting of a new case, the investigators will directly contact reporting clinicians and send them a clinical proforma to collect clinical details about the case. At 12 months, a follow up questionnaire will be sent. The investigators will use only information available from patient case notes, with no direct patient contact. The investigators principal aim is to determine incidence of childhood uveitis in the UK. Secondary aims are to identify presentation patterns, referral pathways, associated medical conditions, management, and outcomes.

Registry
clinicaltrials.gov
Start Date
November 1, 2014
End Date
March 1, 2017
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Any child (aged 0-16 years) with a new diagnosis of uni or bilateral uveitis.

Exclusion Criteria

  • In England/Wales/Northern Ireland, children who are known to have pre existing juvenile idiopathic arthritis (joint inflammation) will be excluded. No exclusions will apply to the Scotland cohort.

Outcomes

Primary Outcomes

The primary outcome measure will be the total number of reported cases of uveitis.

Time Frame: 1 year

A clinical proforma will be sent to the investigators collect clinical details about the case. At 12 months, a followup questionnaire will be sent.

Study Sites (1)

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