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CompletedNCT03753893Updated Apr 12, 2022

Ocular Manifestations in Rheumatic Diseases

An observational study in Uveitis, Conjunctivitis and Keratoconjunctivitis Sicca, sponsored by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's. Completed. Per ClinicalTrials.gov, last updated 2022-04-12.

Sponsored by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Retrospective
Enrollment
5,000
Sex
All
01

Study summary

This is a search strategy for determining the prevalence of ocular complications in inflammatory rheumatic diseases for the purposes of a meta analysis.

Read the detailed description

For the purposes of determining the prevalence of ocular complications in inflammatory rheumatic diseases, the following search terms were used: conjunctivitis, keratoconjunctivitis sicca, xerophthalmia, uveitis, eye hemorrhage, optic neuritis, papilledema, orbital disease, retinal artery/vein occlusion, macular edema, retinitis, chorioretinitis, scleritis, iridocyclitis, choroid hemorrhage, blindness and amaurosis fugax.

These terms were searched in the context of a corresponding inflammatory disease on Medline, Cochrane and Web of Science from their inception (1966, 1991 and 1990 respectively) until the point of study completion.

Studies were included if they provided numerical data of the prevalence or incidence of ocular manifestations in an inflammatory rheumatic disease. Studies were excluded if they were review articles, case reports where all patients experienced the same ocular comorbidity, if different comorbidities were not grouped independently, and if the study reported on fewer than 20 patients. When the same study cohort was used in more than one analysis, the most recent or largest sample-size study was included. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist was used to assess the quality of cohort, case-control, and cross-sectional studies.

02

Conditions studied

  • Uveitis
  • Conjunctivitis
  • Keratoconjunctivitis Sicca
  • Xerophthalmia
  • Eye Hemorrhage
  • Optic Neuritis
  • Papilledema
  • Orbital Diseases
  • Retinal Vein Occlusion
  • Retinal Artery Occlusion
  • Macular Edema
  • Retinitis
  • Chorioretinitis
  • Iridocyclitis
  • Scleritis
  • Choroid Hemorrhage
  • Blindness
  • Amaurosis Fugax
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients with ocular involvement in inflammatory rheumatic disease

Inclusion criteria

  • Studies were included if they provided numerical data of the prevalence or incidence of ocular manifestations in inflammatory rheumatic disease

Exclusion criteria

Exclusion Criteria:

  • review articles,
  • case reports where all patients experienced the same ocular comorbidity
  • if different comorbidities were not grouped independently
  • if the study reported on fewer than 20 patients
04

Study design

Observational model
Ecologic or community
Time perspective
Retrospective
Enrollment
5,000 participants (actual)
Patient registry
No

Interventions

  • OtherNo intervention used

    no intervention used

05

What researchers measure

Primary outcomes

  1. Prevalence of ocular manifestations of inflammatory rheumatic diseases

    Prevalence of ocular manifestations of inflammatory rheumatic diseases

    Time frame: data is collected once per year up to 2020

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03753893
Lead sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Responsible party
Janet Pope (Professor of Medicine, London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's) — Principal investigator
First posted
Nov 27, 2018
Start date
May 1, 2013
Primary completion
Apr 1, 2021
Completion
Nov 1, 2021
Last update
Apr 12, 2022

Study contacts

Janet Pope, MD
principal investigator · London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Oversight

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

Not currently enrolling

This study is completed, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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