Corneal Sensitivity Demographics Study

  • Research type

    Research Study

  • Full title

    Corneal Sensitivity Demographics and its Association with Dry Eye

  • IRAS ID

    318209

  • Contact name

    Michel Guillon

  • Contact email

    MGuillon@otg.co.uk

  • Sponsor organisation

    CooperVision International Limited

  • Duration of Study in the UK

    1 years, 4 months, 18 days

  • Research summary

    The cornea (the clear part of the front of the eye) is the most sensitive part of the body to enable it, as part of its protective mechanism, to trigger a blink if any anomaly is detected. Dry eye, which is the most common eye disease encountered in ophthalmic practice, is due to anomalies of the tear film and / or the ocular surface that lead to a range of ocular symptoms of varying severity. One aspect that is now being investigated is whether corneal sensitivity plays a role in dry eye with the key questions being: i. is corneal sensitivity different in asymptomatic and symptomatic dry eye sufferers; ii. does corneal sensitivity differ for different levels of dry eye severity? To date we do not have an answer to these two key questions, hence the rationale of the proposed population study to compare corneal sensitivity between normal and dry eye sufferers and amongst the latter for different severities.

    The study is an observational, single site, single visit study to measure corneal sensitivity in an adult population, identify the presence or not of dry eye, quantify the type and severity of any dry eye detected. Participants will attend the clinic on one occasion for about two hours. During the visit they will undergo a series of standard clinical tests applied to dry eye patients and corneal sensitivity measurement. Corneal sensitivity measurement is a non-contact test to determine when a participants detects a light intensity puff of air, similar or less in sensation that the puff of air used routinely for the measurement of intraocular pressure by non-contact tonometry. No measurement or research related information is collected before the prospective participant has consented to take part and at the completion of the visit the participants are discharged from the study.

  • REC name

    West Midlands - South Birmingham Research Ethics Committee

  • REC reference

    22/WM/0179

  • Date of REC Opinion

    2 Aug 2022

  • REC opinion

    Further Information Favourable Opinion