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Completed

NCT Number: NCT03395535

Laser-1st vs Drops-1st for Glaucoma and Ocular Hypertension

This is a randomized study with two treatment arms: 'initial Selective Laser Trabeculoplasty (SLT) followed by conventional medical therapy as required' ('Laser-1st') and 'medical therapy without laser ('Medicine-1st'). It compares quality of life in the two arms at three years, while also examining the incremental cost and cost-effectiveness of Laser-1st versus Medicine-1st.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Moorfields Eye Hospital

London, EC1V 2PD, United Kingdom

About this study

Subjects are randomly allocated to one of two treatment arms that examine treatment pathways, rather than comparing single treatments alone: 'initial Selective Laser Trabeculoplasty (SLT) followed by conventional medical therapy as required' ('Laser-1st') and 'medical therapy without laser ('Medicine-1st'). We compare quality of life in the two pathways (arms) over three years, while also examining the incremental cost and cost-effectiveness of Laser-1st versus Medicine-1st.

A 'Treat in Pursuit of Control' design (TPC) compares two different routes to a pre-defined target Intraocular pressure (IOP) (pathways). It is a pragmatic study that uses published guidelines to make the complex clinical treatment choices faced in managing glaucoma, standardised between treatment arms by use of computer treatment algorithms. A UK National Institute for Health and care Excellence (NICE)-compliant evidence-based IOP Treatment Target 1 is set for each patient, according to the study treatment algorithms. They then proceed through stepped increments of treatment intensity (up to and including surgery) until a predetermined Target IOP is reached. Target IOP is reassessed in the light of objective clinical evidence of stability of glaucomatous optic neuropathy (GON) and visual function using visual field tests and automated optic nerve evaluation. Health Related Quality of Life (HRQL) and secondary outcomes are compared for patients in each pathway.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of open angle glaucoma (defined as an open drainage angle and reproducible glaucomatous visual field defects as tested by the Swedish Interactive Threshold Algorithm (SITA) algorithm on the Humphrey Visual Field or glaucomatous optic neuropathy)
  • OR
  • Ocular hypertension (intra-ocular pressure above 21mmHg and requiring treatment as per National Institute of Health and Care Excellence (NICE) Guidelines).
  • Able to provide informed consent.

Exclusion criteria

  • Advanced glaucoma in the potentially eligible eye as determined by Early Manifest Treatment Guidelines (EMGT) criteria 77: visual field loss mean deviation worse than -12dB in the better or -15dB in the worse eye.
  • Secondary glaucoma (e.g. pigment dispersion syndrome, rubeosis, trauma etc) or any angle closure.
  • Any contra-indication to selective laser trabeculoplasty (e.g. unable to sit at the laser-mounted slit-lamp; past history of uveitis).
  • Unable to use topical medical therapy due to e.g. physical infirmity and a lack of carers able to administer daily eye-drops.

Treatment and study plan

Primary Selective Laser Trabeculoplasty Treatment Pathway

Procedure

Primary Selective Laser Trabeculoplasty Treatment (followed by medications as required) Pathway.

First treatment is SLT, 100 shots of laser over 360 degrees. If this does not reach the target IOP then repeat laser (once only) is given. If IOP not at target additional treatment with all standard medications may be used and ultimately surgery (trabeculectomy ).

All available medical treatments (eye-drops) are permitted according to a pre-specified intervention protocol described in detail in the publicly available trial protocol. This begins with prostaglandin analogues, then beta-blockers followed by alpha agonists or carbonic anhydrase inhibitors. The full range of available doses, treatments and drugs is beyond this short summary.

Other names: SLT; "Laser First"

Primary Medical Treatment Pathway

Drug

Primary Medical Treatment Pathway (multiple medications, as required). If IOP not at target additional treatment with all standard medications may be used and ultimately surgery (trabeculectomy ).

All available medical treatments (eye-drops) are permitted according to a pre-specified intervention protocol described in detail in the publicly available trial protocol. This begins with prostaglandin analogues, then beta-blockers followed by alpha agonists or carbonic anhydrase inhibitors. The full range of available doses, treatments and drugs is beyond this short summary.

Other names: Conventional medical therapy; "Medicine First"

Primary outcomes

  1. Health Related Quality of Life using EQ-5D

    Time frame: 3 years

    Quality Adjusted Life Years by EQ-5D health states

Secondary outcomes

  1. Health Related Quality of Life using GUI

    Time frame: 3 years

    Glaucoma-specific treatment-related quality of life: Glaucoma Utility Index (GUI)

  2. Cost-effectiveness ratio

    Time frame: 3 years

    Incremental Cost Effectiveness Ratio

  3. Cost-effectiveness

    Time frame: 3 years

    Cost per Quality Adjusted Life Year (QALY)

  4. Glaucoma Symptom Score (GSS)

    Time frame: 3 years

    Disease and treatment-related symptom score (patient reported outcome, PROM)

  5. Glaucoma Quality of Life-15 (GQL-15)

    Time frame: 3 years

    Patient Reported Visual Function Score (patient reported outcome, PROM)

  6. Glaucoma Utility Index (GUI)

    Time frame: 3 years

    Disease-Specific Utility Score (patient reported outcome, PROM)

  7. Visual Acuity

    Time frame: 3 years

    Visual Function measured using LogMAR acuity.

  8. Humphrey Visual Field Assessments

    Time frame: 3 years

    Visual Function measured using Mean Deviation

  9. Heidelberg Retinal Tomographie optic nerve analysis

    Time frame: 3 years

    Optic nerve structure, measured in mean near-retinal rim width.

  10. Goldmann Applanation Tonometry measured intra-ocular pressure

    Time frame: 3 years

    Clinical outcome of intra-ocular pressure lowering, mmHg.

  11. Hospital visit frequency

    Time frame: 3 years

    Objective measures of treatment pathway efficacy, measured by number of hospital visits in two treatment arms over trial period.

  12. Treatment intensity

    Time frame: 3 years

    Objective measures of treatment pathway efficacy, measured by number of medications used in two treatment arms over trial period.

Sponsors and collaborators

Lead sponsor

Moorfields Eye Hospital NHS Foundation Trust

Other

Registry information

Official study title

Health-Related Quality of Life in Two Pathways for Newly Diagnosed Open Angle Glaucoma and Ocular Hypertension: an Unmasked, Multi-centre, Randomised Controlled Trial of Initial Selective Laser Trabeculoplasty Versus Medical Therapy

Acronym: LIGHT

Important dates

Study start
2012
Primary completion
2017
Study completion
2017
First posted
Jan 10, 2018
Registry last updated
Jan 10, 2018

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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