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OpenTrials
Completed

NCT Number: NCT01983488

Clinical Outcome in Uveitis

This study is aimed at investigating the long term clinical outcome of patients with uveitis.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Moorfields Eye Hospital

London, EC1V 2PD, United Kingdom

About this study

Patients will be included if they are treated for uveitis and have had repeat follow-up. Data will be gathered from the entire length of the patients follow-up.

The main outcome measures will be:

Change from baseline of Best corrected visual acuity (BCVA)at 10 years Causes of vision loss (≤6/15, VL) and severe vision loss (≤6/60, SVL) at 10 years Number of clinical visits at 10 years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical Diagnosis of Uveitis.

Exclusion criteria

  • No follow-up data.

Treatment and study plan

Primary outcomes

  1. Best Corrected Visual Acuity

    Time frame: up to 10 years

    Recorded repeat best corrected visual acuity at intervals throughout the length of follow-up.

Secondary outcomes

  1. Causes of visual loss

    Time frame: First follow-up, years 1,2,5,10, Final follow-up

    Record any ocular changes related to permanent visual loss under 6/12 and severe visual loss under 6/60.

Sponsors and collaborators

Lead sponsor

Moorfields Eye Hospital NHS Foundation Trust

Other

Registry information

Official study title

Clinical Outcome and Causes of Visual Loss in Uveitis

Important dates

Study start
2011
Primary completion
2018
Study completion
2019
First posted
Nov 14, 2013
Registry last updated
Mar 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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