Adaptive Optics in PVR

September 7, 2020 updated by: Moorfields Eye Hospital NHS Foundation Trust

An Observational Study of Retinal Function and Structure After Repair of Macula-involving Retinal Detachment Complicated by Proliferative Vitreoretinopathy (RDPVR) Using Adaptive Optics

The purpose of this study is to investigate the loss of retinal cells following retinal detachment surgery using an imaging device called an adaptive optics camera. The retina is a thin layer which lines the back of the eye. It is sensitive to light (like the film in a camera) and is necessary for vision. If a hole or rip develops in a retina it can become detached. The macula is the central portion of the retina which the investigators use for fine vision. This area can also become detached as part of a retinal detachment. Proliferative vitreoretinopathy (PVR) is an abnormal scarring response inside the eye which can occur when the retina detaches. It can adversely affect the outcome of the retinal detachment repair and is associated with a worse visual prognosis. The investigators want to investigate retinal cell loss in patients with retinal detachments that have developed PVR when the macula has been involved.

The investigators plan to compare them to two other groups of patients, who have not developed PVR:

  1. Patients with macula-involving retinal detachments without PVR
  2. Patients with macula-sparing detachments without PVR

The investigators will investigate retinal cell loss in these types of retinal detachments using adaptive optics imaging. This is a non-invasive imaging technique which allows the investigators to view the retina at very high magnification. Investigating photoreceptor loss and its association with visual outcome in this way should help to guide future interventions in promoting retinal regeneration. The investigators plan to recruit 25 patients at one UK hospital. The project is funded by the charity Fight for Sight.

Study Overview

Status

Completed

Conditions

Detailed Description

A cohort of 10 cases of macula-involving retinal detachment complicated by proliferative vitreoretinopathy grade C (RDPVR group) will be identified from vitreoretinal clinics at Moorfields Eye Hospital. 26 weeks following retinal detachment repair, and after removal of any silicone oil tamponade, these cases will undergo post-operative visual assessment, OCT imaging and microperimetry. These investigations will be correlated with adaptive optics (AO) enface imaging of cone photoreceptors at the macula. This will be compared with groups of 10 cases of macula involving retinal detachment without PVR (RD-OFF) and 5 cases of macula-sparing retinal detachment (RD-ON). Both comparison groups (RD-OFF & RD-ON) will undergo assessments at both 6 weeks and 26 weeks post-operatively.

Study Type

Observational

Enrollment (Actual)

25

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

      • London, United Kingdom
        • Moorfields Eye Hospital NHS Foundation Trust

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with retinal detachments that have developed PVR when the macula has been involved

Description

Inclusion Criteria:

  • RD-PVR group: patients who have had successful retinal surgery to treat macular-involving retinal detachment with PVR C.
  • RD-OFF group: patients who have had successful retinal surgery to treat macular-involving retinal detachment without PVR.
  • RD-ON group: patients who have had successful retinal surgery to treat macular-sparing retinal detachment without PVR.
  • 18 years of age

Exclusion Criteria:

  • Media opacity precluding imaging (including silicone oil tamponade)
  • Poor central fixation (defined as a fixation score of <10 out of 20)
  • Recent contact lens (CLs) wear in the last 48 hours
  • Previous refractive surgery/ other corneal surgery
  • Spherical equivalent refractive error exceeding -12 or +6D
  • Irregularly shaped pupil
  • Unable to be dilated
  • Unable to give informed consent
  • Ocular co-morbidity affecting visual outcome

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

Cohorts and Interventions

Group / Cohort
Macular involving retinal detachment
Patients with retinal detachments that have developed PVR when the macula has been involved

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The difference in cone density in patients following repair of macula-involving retinal detachment in eyes with PVR (RD-PVR), versus macula-involving retinal detachment without PVR (RD-OFF) at 26 weeks following retinal detachment repair.
Time Frame: 6 months
The difference in cone density in patients following repair of macula-involving retinal detachment in eyes with PVR (RD-PVR), versus macula-involving retinal detachment without PVR (RD-OFF) at 26 weeks following retinal detachment repair. Images will be taken with an adaptive optics camera.
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Estimate differences in cone mosaics in the PVR-RD vs RD-OFF groups.
Time Frame: 6 months
Estimate differences in cone mosaics in the PVR-RD vs RD-OFF groups.
6 months
Estimate differences in cone mosaics in the PVR-RD & RD-ON groups.3
Time Frame: 6 months
Estimate differences in cone mosaics in the PVR-RD & RD-ON groups.
6 months
Estimate differences in cone mosaics in the RD-OFF & RD-ON groups
Time Frame: 6 months
Estimate differences in cone mosaics in the RD-OFF & RD-ON groups
6 months
Estimate correlation between cone mosaics and post-operative visual acuity & microperimetry
Time Frame: 6 months
Estimate correlation between cone mosaics and post-operative visual acuity & microperimetry
6 months
Estimate correlation between cone mosaics and retinal layer changes on SD-OCT
Time Frame: 6 months
Estimate correlation between cone mosaics and retinal layer changes on SD-OCT
6 months
Estimate differences in cone mosaics at 6 weeks and 26 weeks following retinal detachment repair (RD-OFF & RD-ON groups only)
Time Frame: 6 months
Estimate differences in cone mosaics at 6 weeks and 26 weeks following retinal detachment repair (RD-OFF & RDIRAS Estimate differences in cone mosaics at 6 weeks and 26 weeks following retinal detachment repair (RD-OFF & RD-ON groups only)
6 months
Exploratory correlation comparison between visual function variables in PVR patients, and various matrices of cone mosaic from AOC
Time Frame: 6 months
Exploratory correlation comparison between visual function variables in PVR patients, and various matrices of cone mosaic from AOC
6 months

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 (Actual)

April 13, 2017

Primary Completion (Actual)

June 4, 2018

Study Completion (Actual)

June 4, 2018

Study Registration Dates

First Submitted

May 10, 2018

First Submitted That Met QC Criteria

June 7, 2018

First Posted (Actual)

June 11, 2018

Study Record Updates

Last Update Posted (Actual)

September 9, 2020

Last Update Submitted That Met QC Criteria

September 7, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CHAD1033

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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