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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03394521
Other study ID # 02/019/15
Secondary ID
Status Completed
Phase N/A
First received May 22, 2017
Last updated March 5, 2018
Start date October 2015
Est. completion date August 2016

Study information

Verified date March 2018
Source University of Aberdeen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to measure how many patients develop worsening glaucoma in the early years (2-4 years) of routine monitoring in hospital eye services. We will study a group of patients who were initially diagnosed as having glaucoma, or having high pressure in the eye (ocular hypertension) or having been diagnosed as a glaucoma suspect.


Description:

In the UK, patients with possible signs of glaucoma or ocular hypertension (OHT) are usually picked up at a routine sight test at their optician or general practitioner. These patients are usually diagnosed in secondary care hospital eye services by an ophthalmologist.

In addition to those diagnosed with OHT and glaucoma there are a large group of patients who have ocular characteristics similar to those found in glaucoma patients, but could also represent variations in normality. In this group, 'glaucoma suspects', monitoring in secondary care for a number of years is recommended in order to establish whether they have glaucoma or if after several years of monitoring there are no clear signs of glaucoma the patient may be discharged.

In our study we will conduct a case-note review of a well-defined cohort of patients who were first identified through a diagnostic accuracy study (the GATE study). This includes (1) patients with OHT, (2) patients identified as glaucoma suspects and (3) patients diagnosed with glaucoma. We will investigate how many patients have experience worsening disease and how many patients have been discharged due to a low risk of glaucoma. We will also investigate the relationship between baseline demographic characteristics and characteristics of the eye and progression of disease.


Recruitment information / eligibility

Status Completed
Enrollment 326
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Eligibility for patients to be recruited into the GATE study was as follows:

Inclusion criteria:

- Adults referred from community optometrists or general practitioner to hospital eye services with suspected glaucoma, including those with ocular hypertension.

Exclusion criteria:

- Patients referred to hospital eye services because of other ocular disease;

- patients < 18 years old;

- patients who cannot give informed consent,

- patients already diagnosed with glaucoma.

This study cohort is further defined from the GATE population as

Selection criteria:

- GATE study patients with a baseline diagnosis of OHT, Glaucoma suspect or Glaucoma (any mechanism);

- remaining in secondary care monitoring after first visit;

- recruited at Aberdeen Royal Infirmary or Hinchingbrooke Hospital NHS Trust.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Routine clinical practice
This is an observational study

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Aberdeen Queen's University, Belfast

Outcome

Type Measure Description Time frame Safety issue
Primary Development of glaucoma Proportion of glaucoma suspects and OHT patients who develop glaucoma annually up to 4 years after diagnosis in secondary care 4 years
Secondary Progression of glaucoma Proportion of the cohort of glaucoma patients with progression of disease up to 4 years 1,2,3,4 years
Secondary Predictors of disease progression Evaluation of predictors of disease progression from baseline demographic and ocular characteristics 4 years
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