Brief Summary

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

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2013

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2013

Completed
5.5 years until next milestone

First Submitted

Initial submission to the registry

October 31, 2018

Completed
27 days until next milestone

First Posted

Study publicly available on registry

November 27, 2018

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2021

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2021

Completed
Last Updated

April 12, 2022

Status Verified

April 1, 2022

Enrollment Period

7.9 years

First QC Date

October 31, 2018

Last Update Submit

April 11, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • Prevalence of ocular manifestations of inflammatory rheumatic diseases

    Prevalence of ocular manifestations of inflammatory rheumatic diseases

    data is collected once per year up to 2020

Interventions

no intervention used

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with ocular involvement in inflammatory rheumatic disease

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

UveitisConjunctivitisKeratoconjunctivitis SiccaXerophthalmiaEye HemorrhageOptic NeuritisPapilledemaOrbital DiseasesRetinal Vein OcclusionRetinal Artery OcclusionMacular EdemaRetinitisChorioretinitisIridocyclitisScleritisChoroid HemorrhageBlindnessAmaurosis Fugax

Condition Hierarchy (Ancestors)

Uveal DiseasesEye DiseasesConjunctival DiseasesKeratoconjunctivitisKeratitisCorneal DiseasesDry Eye SyndromesLacrimal Apparatus DiseasesHemorrhagePathologic ProcessesPathological Conditions, Signs and SymptomsEye ManifestationsSigns and SymptomsOptic Nerve DiseasesCranial Nerve DiseasesNervous System DiseasesRetinal DiseasesVenous ThrombosisThrombosisEmbolism and ThrombosisVascular DiseasesCardiovascular DiseasesArterial Occlusive DiseasesMacular DegenerationRetinal DegenerationChoroiditisChoroid DiseasesUveitis, PosteriorPanuveitisIris DiseasesUveitis, AnteriorScleral DiseasesVision DisordersSensation DisordersNeurologic Manifestations

Study Officials

  • Janet Pope, MD

    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Medicine

Study Record Dates

First Submitted

October 31, 2018

First Posted

November 27, 2018

Study Start

May 1, 2013

Primary Completion

April 1, 2021

Study Completion

November 1, 2021

Last Updated

April 12, 2022

Record last verified: 2022-04

Data Sharing

IPD Sharing
Will not share