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MYOPRED
Sponsor study identifier
observational
609
1 country
1
Study Start
April 27, 2017
Actual (reported)Primary Completion
October 30, 2024
Actual (reported)Study Completion
September 14, 2025
Actual (reported)Phacoemulsification with implantation of posterior chamber lenses represents the gold standard of care for patients needing lens surgery, but there is an increased risk of developing pseudophakic retinal detachment after surgery. Especially myopic patients have an even higher risk of pseudophakic retinal detachment compared to the general population. The aim of this multicenter study is to document the presence and/or post-operative development of posterior vitreous detachment (PVD) and to assess its influence on the incidence of retinal detachment (RD) in myopes in a time period of three and five years after lens surgery. 618 eyes of patients scheduled for regular lens surgery will be included, defined by an axial length of 25.0 mm or more. To examine the vitreous status, all patients will receive a comprehensive eye examination pre-operatively, including funduscopy with assessment of a Weiss ring and optical coherence tomography (OCT). Patients will be divided into two groups, group A with pre-operative complete PVD and group B with no/partial PVD. Group A will be invited for one follow-up visit (two months post-operatively) followed up by telephone interviews at one, two, three and five years after surgery to determine occurrence of pseudophakic retinal detachment. Group B will be invited for follow-up examinations at two months, six months and one year after surgery to document occurrence of PVD (if a PVD is present at one of the follow-ups, no more visits are necessary). Two, three and five years after surgery, all patients from group B will be interviewed by telephone, as in group A, to document the occurrence of pseudophakic retinal detachment. In the recent literature the association between the occurrence of PVD pre-/post-operative and RD after lens surgery is well documented but not described for myopic patients. The results of this multicenter study should help to tackle the problem of RD prediction in myopic patients depending on their pre-operative vitreous status, especially in the setting of refractive lens exchange.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
September 14, 2025
Actual (reported)Click on a node to explore related trials.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
April 19, 2017
Actual (reported)April 27, 2017
Actual (reported)May 15, 2017
Actual (reported)October 30, 2024
Actual (reported)September 14, 2025
Actual (reported)PVD status
Number of patients with preoperative and/or post-operatively developed posterior vitreous detachment (PVD)
1 year
Incidence of RD
Influence of PVD on the incidence of retinal detachment (RD) in myopes after lens surgery.
5 years
Study population: target 618. The participants will be selected by the clinical investigators at several ophthalmological centres in Austria, Belgium, Spain, Norway and the Netherlands. As the study population is already scheduled for cataract surgery / refractive lens exchange, recruitment will be performed directly in these centres at the pre-assessment visits. At this visit, optical biometry is performed and patients with suitable axial eye lengths will be screened. If all inclusion and no exclusion criteria are met the patients will be asked to participate in the trial.
Vienna Institute for Research in Ocular Surgery
Vienna, State of Vienna, 1140, Austria
Oliver Findl, Prof. Dr.
Vienna Institute for Research in Ocular Surgery
609 participants (actual enrollment reported by the registry).
First Submitted
April 19, 2017
First Posted
May 15, 2017
Study Start
April 27, 2017
Actual (reported)Contact the study team to confirm eligibility.
Primary Completion
October 30, 2024
Actual (reported)Study Completion
September 14, 2025
Actual (reported)Last Updated
March 13, 2026
Record last verified: 2026-03
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Source: ClinicalTrials.gov.
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