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Completed

NCT Number: NCT05171621

Measuring Subjective Quality of Vision and Metamorphopsia Before and After Epiretinal Membrane and Macular Hole Surgery

Assessing metamorphopsia and quality of vision pre and post epiretinal and macular hole surgery

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Wales

Cardiff, cf14 4xw, United Kingdom

About this study

Metamorphopsia is a visual symptom in which straight lines appear distorted, for example a vertical window blind may appear wavy which can affect quality of vision. Metamorphopsia is a common symptom in retinal conditions such as epiretinal membranes (ERM) and macular holes. There is a lack of studies analysing the prevalence of ERM in the UK and Europe.

Both of the conditions have shown to be a higher risk factor with age. With an aging population it is likely these numbers will increase. Currently the only treatment option is surgery (vitrectomy) or conservative management to monitor the condition. It would therefore be beneficial to find a tool that would inform the surgeon of a patient's quality of vision and how this impacts their life. A patient's severity of metamorphopsia reveals more precise information on the progression of the disease than visual acuity alone (Nomoto et al. 2013) therefore gaining a better understanding can help aid clinical decisions.

Current clinical practice is to monitor metamorphopsia with an Amsler chart, a grid with lines; the patient is then asked to draw where they can see distortion. They are used to detect metamorphopsia but are unable to quantify and provide an accurate measurement of the severity of metamorphopsia and quality of vision

The Quality of Vision questionnaire (QoV) (McAlinden et al. 2010) is a modern tool developed to specifically measure subjective quality of vision. The Metamorphopsia questionnaire (Arimura et al. 2011) has been developed to provide a measurement of subjective metamorphopsia in macular disease. Both have been psychometrically validated and are in use in a number of clinical trials worldwide.

It would be valuable to investigate the role of each questionnaire in identifying quality of vison and metamorphopsia pre- and post-surgery for ERM and macular holes to establish if there are changes to patient responses. We would compare this to visual acuity and optical coherence tomography (OCT) images pre- and post-surgery to see if changes correspond to the questionnaire responses. If a questionnaire can measure metamorphopsia and its impact on quality of vision in ERM and macular holes, this would assist in clinical decision making.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Participant is willing and able to give informed consent
  • >18 years old
  • Patients listed for epi retinal and macular hole surgery
  • Patient is able to perform study procedures

Exclusion criteria

  • Patients who are diagnosed with a condition other than epiretinal membrane or macular hole
  • Patients not undergoing epiretinal or macular hole surgery
  • Patients will be excluded if there are any complications within surgery, or undergo any procedures that is not an epiretinal or macular hole surgery (i.e vitrectomy, phacoemulsification (lens extraction) as this can affect visual outcomes.

Treatment and study plan

Primary outcomes

  1. Compare the responses of the McAllinden and Metamorphopsia Questionnaire

    Time frame: pre surgery and 2 - 3 months post surgery

    analysing changes to responses in the 2 questionnaires pre and post surgery

Secondary outcomes

  1. Changes to BCVA score

    Time frame: Pre surgery and 2-3 months post surgery

    Patients BCVA pre and post surgery to see if there is an improvement

Other outcomes

  1. Assess correlations between the Mcallinden and Metamorphopsia questionnaire scores and objective clinical parameters

    Time frame: Pre surgery and 2-3 month post surgery

    do the questionnaires show changes pre and post surgery and do they match clinical outcomes

Sponsors and collaborators

Lead sponsor

Hayley Westwood

Other

Registry information

Acronym: MQUEST

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Dec 29, 2021
Registry last updated
Dec 29, 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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