Proteomic Profiles in Trabeculectomy Patients

October 29, 2018 updated by: Louis Tong, Singapore National Eye Centre

Long-term Observation of Tear Proteomic Profiles and Ocular Surface in Trabeculectomy Patients Before and After Surgery

Approximately 70 million people world-wide are affected with glaucoma, of whom 6.7 million have bilateral blindness.5 Elevated intro-ocular pressure is the major modifiable risk factor in glaucoma, and reducing intraocular pressure to a consistently low level can delay disease progression and therefore, blindness.6 Topical intraocular pressure -lowering medication remains the first-line treatment for glaucoma, with surgical intervention playing a secondary role in cases suboptimally controlled with medication alone.

In this study, we plan to assess the change in tear proteins in trabeculectomy patients before and after operations. It is hoped that this study could help us gain more understanding of the possible mechanism accounting for the development of dry eye disease in glaucoma patients, which could help us develop better screening modalities and therapeutic agents for glaucoma patients at risk to prevent the development of dry eye disease.

Study Overview

Status

Completed

Conditions

Detailed Description

Study Objectives and Purpose

There are two primary aims in this study:

  1. To assess changes in the tear proteomic profiles in pre-trabeculectomy and post-trabeculectomy patients
  2. To assess the changes in clinical signs of the eye and tear film as well as dry eye symptoms.

Study Material Human Tears will be collected from patients in SNEC clinic

Study Design:

120 patients will be recruited for this study (details as described below). Schirmers I test, Tear Osmolarity, Tear Break Up Time (TBUT), Anterior segment optical coherence tomography (ASOCT) and Impression cytology will be done during the study visits. Subjective symptom and severity of dry eye disease will be assessed through Visual Analog Scale (VAS).

No. of visits:

There will be 4 visits in this study. Visit 1: Pre-trabeculectomy operation Visit 2: 6 month after trabeculectomy surgery Visit 3: 1 year after trabeculectomy surgery Visit 4: 3 years after trabeculectomy surgery

Selection and Withdrawal of Subjects Recruitment Criteria

  1. 120 patients will be recruited from glaucoma clinics in SNEC
  2. Patients age ≥ 21 years old
  3. Patients who require trabeculectomy operation

Treatment of subjects

Study Procedures:

  1. Fluorescein staining will be used to visualize patient eyes.
  2. Schirmer's test will be used to measure the amount of tear production

    1. A small strip of filter paper will be inserted inside the lower eyelid
    2. A topical aneasthetic is placed into the eye before the filter paper to prevent tearing due to the irritation from the paper
    3. The eyes are closed for 5 minutes.
    4. The paper is then removed and the amount of moisture is measured
  3. Impression cytology will be performed to collect the superficial conjunctival cells for analysis

    1. While the eye is still anaesthetized from Schirmer's test, one end of a filter paper will be impressed upon the temporal conjunctiva whilst the other hand is grasped in place with a blunt smooth edged forceps.
    2. The filter paper is removed from the conjunctiva with a peeling motion after 2-3 seconds.
    3. The paper is placed into an eppendorf tube for future analysis.
  4. Tear osmolarity, Tear Break Up Time (TBUT) will be measured in all patients

    a) Tear osmolarity will be measured using the osmolarity chip, 3 chips per eye

  5. Anterior segment optical coherence tomography will be performed to assess the tear meniscus and image for any conjunctivochalasis

    a) The patient will be asked to look at a target in the instrument while blinking normally. The instrument will scan the lower eyelid margin for imaging of the tear meniscus and conjunctivochalasis

  6. Symptoms and severity of dry eye disease will be assessed through the Visual Analog Scale (VAS) system

Assessment of efficacy Outcome Measures

  1. Symptoms and severity of dry eye disease will be quantified based on the Visual Analog Scale (VAS)11
  2. Amount of moisture of the filter paper will be measured in Schirmer's test
  3. Clinical assessment of dry eye disease through Tear break up time (TBUT) and Tear Osmolarity measurements
  4. Tear meniscus height and area in the images obtained with optical coherence tomography

Target sample size 120 subjects will be enrolled in the study.

Study Type

Observational

Enrollment (Actual)

36

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Singapore, Singapore, 168751
        • Singapore National Eye Centre/ Singapore Eye Research Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years to 99 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

120 patients will be recruited for this study

Description

Inclusion Criteria:

  1. 120 patients will be recruited from glaucoma clinics in SNEC
  2. Patients age ≥ 21 years old
  3. Patients who require trabeculectomy operation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change from baseline in the tear protein profiles in trabeculectomy patients at 3 years
Time Frame: Baseline and 3 years
Baseline and 3 years

Secondary Outcome Measures

Outcome Measure
Time Frame
Symptoms and severity of dry eye disease
Time Frame: Baseline and 3 years
Baseline and 3 years
Amount of tears will be measured
Time Frame: Baseline and 3 years
Baseline and 3 years
Tear Osmolarity will be measured
Time Frame: Baseline and 3 years
Baseline and 3 years
Tear meniscus height will be measured
Time Frame: Baseline and 3 years
Baseline and 3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2013

Primary Completion (Actual)

October 1, 2018

Study Completion (Actual)

October 1, 2018

Study Registration Dates

First Submitted

April 19, 2013

First Submitted That Met QC Criteria

April 25, 2013

First Posted (Estimate)

April 26, 2013

Study Record Updates

Last Update Posted (Actual)

October 31, 2018

Last Update Submitted That Met QC Criteria

October 29, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • R980/89/2012
  • 2013/020/A (Other Identifier: Singhealth Centralised Institutional Review Board)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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