Effect of medically lowering intraocular pressure in glaucoma suspects with high myopia (GSHM study): study protocol for a randomized controlled trial.
Glaucoma suspect
High myopia
Intraocular pressure
Randomized controlled trial
Journal
Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253
Informations de publication
Date de publication:
29 Sep 2020
29 Sep 2020
Historique:
received:
22
04
2020
accepted:
17
09
2020
entrez:
30
9
2020
pubmed:
1
10
2020
medline:
22
6
2021
Statut:
epublish
Résumé
Currently, whether and when intraocular pressure (IOP)-lowering medication should be used in glaucoma suspects with high myopia (GSHM) remains unknown. Glaucoma suspects are visual field (VF) defects that cannot be explained by myopic macular changes or other retinal and neurologic conditions. Glaucoma progression is defined by VF deterioration. Here we describe the rationale, design, and methodology of a randomized controlled trial (RCT) designed to evaluate the effects of medically lowering IOP in GSHM (GSHM study). The GSHM study is an open-label, single-center, RCT for GSHM. Overall, 264 newly diagnosed participants, aged 35 to 65 years, will be recruited at the Zhongshan Ophthalmic Center, Sun Yat-sen University, between 2020 and 2021. Participants will be randomly divided into two arms at a 1:1 ratio. Participants in the intervention arm will receive IOP-lowering medication, while participants in the control arm will be followed up without treatment for 36 months or until they reach the end point. Only one eye per participant will be eligible for the study. If both eyes are eligible, the eye with the worse VF will be recruited. The primary outcome is the incidence of glaucoma suspect progression by VF testing over 36 months. The secondary outcomes include the incidence of changes in the optic nerve head morphology including the retinal nerve fiber layer, and retinal ganglion cell-inner plexiform layer loss, progression of myopic maculopathy, visual function loss, and change in the quality of life. Statistical analyses will include baseline characteristics comparison between the intervention and control groups using a two-sample t-test and Wilcoxon rank sum test; generalized linear models with Poisson regression for the primary outcome; Kaplan-Meier curve and log-rank test for the incidence of the secondary outcome; and longitudinal analyses to assess trends in outcomes across time. To the best of our knowledge, the GSHM study is the first RCT to investigate the impact of medically lowering IOP in GSHM. The results will have implications for the clinical management of GSHM. ClinicalTrials.gov NCT04296916 . Registered on 4 March 2020.
Sections du résumé
BACKGROUND
BACKGROUND
Currently, whether and when intraocular pressure (IOP)-lowering medication should be used in glaucoma suspects with high myopia (GSHM) remains unknown. Glaucoma suspects are visual field (VF) defects that cannot be explained by myopic macular changes or other retinal and neurologic conditions. Glaucoma progression is defined by VF deterioration. Here we describe the rationale, design, and methodology of a randomized controlled trial (RCT) designed to evaluate the effects of medically lowering IOP in GSHM (GSHM study).
METHODS
METHODS
The GSHM study is an open-label, single-center, RCT for GSHM. Overall, 264 newly diagnosed participants, aged 35 to 65 years, will be recruited at the Zhongshan Ophthalmic Center, Sun Yat-sen University, between 2020 and 2021. Participants will be randomly divided into two arms at a 1:1 ratio. Participants in the intervention arm will receive IOP-lowering medication, while participants in the control arm will be followed up without treatment for 36 months or until they reach the end point. Only one eye per participant will be eligible for the study. If both eyes are eligible, the eye with the worse VF will be recruited. The primary outcome is the incidence of glaucoma suspect progression by VF testing over 36 months. The secondary outcomes include the incidence of changes in the optic nerve head morphology including the retinal nerve fiber layer, and retinal ganglion cell-inner plexiform layer loss, progression of myopic maculopathy, visual function loss, and change in the quality of life. Statistical analyses will include baseline characteristics comparison between the intervention and control groups using a two-sample t-test and Wilcoxon rank sum test; generalized linear models with Poisson regression for the primary outcome; Kaplan-Meier curve and log-rank test for the incidence of the secondary outcome; and longitudinal analyses to assess trends in outcomes across time.
DISCUSSION
CONCLUSIONS
To the best of our knowledge, the GSHM study is the first RCT to investigate the impact of medically lowering IOP in GSHM. The results will have implications for the clinical management of GSHM.
TRIAL REGISTRATION
BACKGROUND
ClinicalTrials.gov NCT04296916 . Registered on 4 March 2020.
Identifiants
pubmed: 32993769
doi: 10.1186/s13063-020-04748-7
pii: 10.1186/s13063-020-04748-7
pmc: PMC7525951
doi:
Banques de données
ClinicalTrials.gov
['NCT04296916']
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
813Subventions
Organisme : High-level Hospital Construction Project, Zhongshan Ophthalmic Center, Sun Yat-sen University
ID : 303020104
Investigateurs
Xiu Lan Zhang
(XL)
Yi Zhi Liu
(YZ)
Lin Lv
(L)
David S Friedman
(DS)
Jost B Jonas
(JB)
Tin Aung
(T)
Shi Da Chen
(S)
Wei Wang
(W)
Feng Bin Lin
(FB)
Yun He Song
(YH)
Fei Li
(F)
Kai Gao
(K)
Bing Qian Liu
(BQ)
Yu Hong Liu
(YH)
Mei Ling Chen
(ML)
Neil M Bressler
(NM)
Ki Ho Park
(KH)
Ming Guang He
(MG)
Ching-Yu Cheng
(CY)
Paul Healey
(P)
Xiang Chen
(X)
Guang Xian Tang
(GX)
Ling Jin
(L)
Références
Br J Ophthalmol. 2019 Oct;103(10):1347-1355
pubmed: 31040131
Ophthalmology. 2006 Sep;113(9):1603-12
pubmed: 16949445
Ophthalmology. 2011 Oct;118(10):1989-1994.e2
pubmed: 21684603
Invest Ophthalmol Vis Sci. 2018 Sep 4;59(11):4691-4700
pubmed: 30267091
Am J Ophthalmol. 2006 Oct;142(4):576-82
pubmed: 17011848
Ophthalmology. 2007 Feb;114(2):216-20
pubmed: 17123613
Ophthalmology. 2013 Feb;120(2):284-91
pubmed: 23084122
Ophthalmology. 2013 Jan;120(1):68-76
pubmed: 22986112
Invest Ophthalmol Vis Sci. 2019 Mar 1;60(4):1096-1104
pubmed: 30901386
Invest Ophthalmol Vis Sci. 2017 Nov 1;58(13):5897-5906
pubmed: 29164230
Retina. 2020 Mar;40(3):399-411
pubmed: 31259808
Br J Ophthalmol. 2018 Jul;102(7):855-862
pubmed: 29699985
Lancet. 2015 Apr 4;385(9975):1295-304
pubmed: 25533656
Ophthalmology. 2005 Oct;112(10):1661-9
pubmed: 16111758
Am J Ophthalmol. 2015 May;159(5):877-83.e7
pubmed: 25634530
Am J Ophthalmol. 1998 Oct;126(4):487-97
pubmed: 9780093
Am J Ophthalmol. 2000 Oct;130(4):429-40
pubmed: 11024415
Invest Ophthalmol Vis Sci. 2012 Nov 01;53(12):7504-9
pubmed: 23060137
PLoS One. 2017 Apr 5;12(4):e0175120
pubmed: 28380081
Ophthalmology. 1999 Nov;106(11):2144-53
pubmed: 10571351
Ophthalmology. 2014 Mar;121(3):682-92.e2
pubmed: 24326106
Ophthalmology. 2016 Jan;123(1):P112-51
pubmed: 26581560
Arch Ophthalmol. 2002 Oct;120(10):1268-79
pubmed: 12365904
Invest Ophthalmol Vis Sci. 2018 May 1;59(6):2644-2651
pubmed: 29847673