Effect of medically lowering intraocular pressure in glaucoma suspects with high myopia (GSHM study): study protocol for a 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
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

813

Subventions

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)

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Auteurs

Feng Bin Lin (FB)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Shi Da Chen (S)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Yun He Song (YH)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Wei Wang (W)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Ling Jin (L)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Bing Qian Liu (BQ)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Yu Hong Liu (YH)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Mei Ling Chen (ML)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Kai Gao (K)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

David S Friedman (DS)

Massachusetts Eye and Ear, Harvard University, Boston, USA.

Jost B Jonas (JB)

Department of Ophthalmology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Tin Aung (T)

Singapore National Eye Center, Singapore, Singapore.

Lin Lv (L)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Yi Zhi Liu (YZ)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China.

Xiu Lan Zhang (XL)

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, No.7, Jinsui Road, Guangzhou, 510060, China. zhangxl2@mail.sysu.edu.cn.

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Classifications MeSH