Long-term clinical management of neovascular AMD and visual acuity outcome in IVAN trial participants
Long-term clinical management of neovascular AMD and visual acuity outcome in IVAN trial participants
Purpose: To describe treatment frequency for neovascular age-related macular degeneration (nAMD), and visual acuity, in IVAN trial participants in the UK’s national health service during the 5 to 7 years since exiting the IVAN trial.
Methods: This extension studied participants who completed the IVAN clinical trial. Consent at enrolment allowed for collection of clinical data beyond trial exit but not for further research visits. A new ethics approval allowed surviving participants to be invited to attend a study visit, extraction of usual care visit data if they did not wish to attend and for deceased participants. We examined the medical records from trial exit (04/2010-11/2012) to end of follow-up (04/2016-06/2017) for usual care and research visits, extracting: visit date; distance visual acuity (DVA) for both study and fellow eyes; treatments for nAMD administered to either eye. We derived duration of study eye monitoring and …
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Reeves, Barney
3b9ef9f2-13c0-4ad2-af9e-378b33725cfd
Evans, Rebecca
05e323ee-05fa-4f47-a9d2-420bb1fe22af
Harding, Simon P.
10091207-4f52-491b-b069-98bb37444f5b
Lotery, Andrew
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514
22 July 2019
Reeves, Barney
3b9ef9f2-13c0-4ad2-af9e-378b33725cfd
Evans, Rebecca
05e323ee-05fa-4f47-a9d2-420bb1fe22af
Harding, Simon P.
10091207-4f52-491b-b069-98bb37444f5b
Lotery, Andrew
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514
Reeves, Barney, Evans, Rebecca, Harding, Simon P. and Lotery, Andrew
(2019)
Long-term clinical management of neovascular AMD and visual acuity outcome in IVAN trial participants.
Investigative Ophthalmology & Visual Science, 60 (9), .
Record type:
Meeting abstract
Abstract
Purpose: To describe treatment frequency for neovascular age-related macular degeneration (nAMD), and visual acuity, in IVAN trial participants in the UK’s national health service during the 5 to 7 years since exiting the IVAN trial.
Methods: This extension studied participants who completed the IVAN clinical trial. Consent at enrolment allowed for collection of clinical data beyond trial exit but not for further research visits. A new ethics approval allowed surviving participants to be invited to attend a study visit, extraction of usual care visit data if they did not wish to attend and for deceased participants. We examined the medical records from trial exit (04/2010-11/2012) to end of follow-up (04/2016-06/2017) for usual care and research visits, extracting: visit date; distance visual acuity (DVA) for both study and fellow eyes; treatments for nAMD administered to either eye. We derived duration of study eye monitoring and …
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Published date: 22 July 2019
Identifiers
Local EPrints ID: 433974
URI: http://eprints.soton.ac.uk/id/eprint/433974
ISSN: 0146-0404
PURE UUID: 06dc8052-4c22-4a7b-be1f-4386f11b6169
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Date deposited: 09 Sep 2019 16:30
Last modified: 17 Mar 2024 02:57
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Author:
Barney Reeves
Author:
Rebecca Evans
Author:
Simon P. Harding
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