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'Distortion as a Predictor of ERM Surgery Outcome'

Does Pre-operative D-chart Score Predict Improvement in VFQ-25 Score Following Surgery for Epiretinal Membrane?

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04791631
Enrollment
60
Registered
2021-03-10
Start date
2021-04-01
Completion date
2023-04-01
Last updated
2021-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Distortion, Epiretinal Membrane, Quality of Life

Brief summary

Epiretinal membranes (ERM) consist of an abnormal growth of tissue across the retina and are present about 6% of people aged 50 and over. They can cause symptoms of distortion (straight lines appearing bent) or blurred vision. Management options include observation if asymptomatic, or surgery to peel the membrane if symptomatic. Limited data exists regarding how to identify patients who are most likely to benefit from surgery. We propose to measure the effects on distortion (using D chart), visual acuity and vision-related quality of life (using a validated vision-related quality of life questionnaire) of ERM surgery. This will allow us to investigate whether pre-operative D chart score can predict subsequent improvement in quality of life following surgery. We hope the results will help patients and VR surgeons decide whether or not to proceed with ERM surgery. The study will be a prospective case series consisting of patients with symptomatic epiretinal membranes who choose to have epiretinal membrane surgery. The study participants will get standard care with the additional administration of a quality of life questionnaire and measurement of distortion (using a D-chart) at 3 different time points (pre-op, and post-op at 26 and 52 weeks). Recruitment will be in Glasgow, with a possibility of other sites being added on at a later stage.

Detailed description

Epiretinal membranes consist of a proliferation of fibrocellular tissue along the inner aspect of the retina. Over time, this membrane can result in anterior-posterior traction and cause disruption of the retinal architecture, which can lead to symptoms of blurred vision, or distorted vision (with straight lines appearing bent or wavy). Patients with ERM now constitute one of the most common referrals to the vitreoretinal service. Management of epiretinal membrane includes observation or surgery for severely symptomatic membranes. The surgery consists of vitrectomy and epiretinal +/- inner limiting membrane peel. Currently there is limited evidence to help identify which patients with an epiretinal membrane are the most likely to benefit from this operation, which makes it more difficult for patients to be able to weigh up the benefits and risks of proceeding with this elective procedure. Our study will measure the effects on distortion (using D chart), visual acuity and quality of life of ERM surgery. Hence it will allow us to investigate whether the pre-op D chart score can predict subsequent improvement in quality of life following surgery. This will provide vitreoretinal surgeons and patients with an evidence base regarding the success of this elective procedure and offer realistic expectations regarding surgical outcomes. Ultimately, we hope that the results of this study will facilitate the decision of whether or not to proceed with ERM surgery. We plan to recruit patients with an epiretinal membrane who choose to undergo surgery at the time of their clinic appointment within the vitreoretinal service. In addition to standard care, the study participants will undergo measurements of distortion (using a D-chart, duration 5-10 minutes) and fill in a quality of life questionnaire. These measurements will be taken before the operation and at six and twelve months following the operation. The aims of the study are: * To investigate the sustained effect of epiretinal membrane surgery on distortion (using D-chart), visual acuity and vision-related quality of life (using NEI VFQ-25 questionnaire) * To determine the relationship between pre-operative distortion score and post-operative vision-related quality of life score following ERM surgery Our study will have a larger number of participants with a longer period of follow up (52 weeks) than comparable studies. It will be the first epiretinal membrane study that measures distortion using the D-chart, which we believe to be superior to existing tests (such as the M-chart) which have been used in similar studies.

Interventions

Surgery for epiretinal membrane i.e. standard 3-port pars plana vitrectomy and epiretinal membrane and internal limiting membrane peel. Phakic patients will undergo cataract surgery.

Sponsors

Royal College of Surgeons of Edinburgh
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Idiopathic epiretinal membrane 2. Patients undergoing vitrectomy and gas surgery, under local or general anaesthetic 3. Able to give informed consent 4. 18 years old and over

Exclusion criteria

1. Epiretinal membrane secondary to retinal detachment, uveitis or retinal vascular disease 2. Previous vitreoretinal surgery 3. Pre-existing ophthalmic condition which limits the patient's visual acuity (Documented BCVA 6/36 or worse) 4. Pre-existing ophthalmic conditions which cause metamorphopsia (exudative ARMD, central serous retinopathy) 5. VA \< 6/60

Design outcomes

Primary

MeasureTime frameDescription
VFQ-25 score at final visit (52 weeks after ERM surgery)1 yearMeasure of vision-related quality of life using NEI VFQ-25 quality of life questionnaire, 1 year after surgery for epiretinal membrane

Secondary

MeasureTime frameDescription
Distortion score pre-operatively and at 26 and 52 weeks after ERM surgery1 yearDistortion score calculated using D-chart
Best-corrected visual acuity pre-operatively and at 26 and 52 weeks after ERM surgery1 yearVisual acuity measured in ETDRS
Vision-related quality of life pre-operatively and at 26 and 52 weeks after ERM surgery1 yearVision-related quality of life assessed using NEI VFQ-25 quality of life questionnaire
Central retinal thickness pre-operatively and at 26 and 52 weeks after ERM surgery1 yearCentral retinal thickness obtained from OCT scans done in clinic

Countries

United Kingdom

Contacts

Primary ContactEmma McDonough
Emma.McDonough@ggc.scot.nhs.uk+44141 314 4000
Backup ContactLona Jawaheer
lonajawaheer@nhs.net+447783520779

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026