Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Mr Mark Wilkins
+44 (0)20 7566 2036
mail@markwilkins.co.uk


Study Location:

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Be Part of Research - Trial Details - A prospective randomised controlled trial comparing bilateral multifocal intraocular lens implantation with monovision following cataract surgery

A prospective randomised controlled trial comparing bilateral multifocal intraocular lens implantation with monovision following cataract surgery

Not Recruiting

Open to: All Genders

Age: Adult

Medical Conditions

Cataract


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Not provided at time of registration

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

01 Feb 2007 01 Feb 2009

Publications

2013 Results article in http://www.ncbi.nlm.nih.gov/pubmed/24070808 results

Interventional

Intervention Type : Device
Intervention Description : Bilateral intraocular lens implant with either TECNIS ZM000 multifocal or Bausch and Lomb Akreos AO monofocal intraocular lenses.




You can take part if:



You may not be able to take part if:


1. Patients aiming for a refractive result other than bilateral emmetropia (0.00 to -0.50D spherical equivalant) or emmetropia in one eye and low myopia in the other, i.e., the intended monovision outcome2. Significant co-pathology (including macular pathology, glaucoma, uveitis, corneal disease, diabetic retinopathy, previous retinal detachment surgery)3. Keratometric astigmatism 1.5D in either eye4. Amblyopia5. Congenital or traumatic cataracts6. Poor comprehension of written or spoken English7. Inability to give informed consent8. Mobility, tremor or postural problems causing discomfort during slit lamp examination


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Moorfields Eye Hospital NHS Foundation Trust
    London
    EC1V 2PD

This information has not yet been provided by the study team. You'll have an opportunity to discuss any risks and benefits that may be associated with this study prior to consenting to taking part.


The study is sponsored by Moorfields Eye Hospital NHS Foundation Trust (UK) and funded by Advanced Medical Optics (AMO) United Kingdom Ltd (UK); Bausch & Lomb UK Ltd (UK).




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What will you do next?

Read full details for Trial ID: ISRCTN37400841
Last updated 08 April 2015

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