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Posterior Capsule Opacification After Lens Capsule Polishing

Evaluation of Intraoperative Capsular Polishing on Lens Epithelial Cells and the Development of Posterior Capsule Opacification

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03857412
Enrollment
40
Registered
2019-02-28
Start date
2019-02-13
Completion date
2021-02-01
Last updated
2020-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Capsule Opacification

Keywords

Polishing, Cataract surgery

Brief summary

Investigate the effect of polishing of the lens capsule during cataract surgery on the development of posterior capsule opacification

Detailed description

Cataract, the clouding if the eye's lens, is the leading cause of blindness worldwide, with phacoemulsification and implantation of an intraocular lens being the only therapeutic option. Cataract surgery is nowadays considered a safe and efficient procedure. However, one of the most frequent complications after surgery is posterior capsule opacification (PCO), that results in diminished postoperative visual acuity. PCO occurs due to remaining lens epithelial cells in the capsular bag, that start to migrate and proliferate. PCO can be easily treated by performing a neodymium-doped yttrium aluminium garnet (Nd-YAG) laser capsulotomy. However, even if laser capsulotomy is considered a simple procedure, possible complications are rise of intraocular pressure, inflammation, cystoid macular edema, or retinal detachment. Furthermore, several patients are no suitable candidates for laser capsulotomy, for example children and patients with high myopia. Therefore, it would be necessery to identify different approaches to prevent generation of PCO. One approach could be cleaning of the lens epithelial cells in the capsular bag by polishing of the lens capsule during surgery. Hence, the aim of this study is to examine whether capsular polishing is beneficial to decrease the growth and proliferation of LECs.

Interventions

PROCEDURECapsular polishing

Capsular polishing taking place during cataract surgery

OTHERNon capsular polishing

No capsular polishing taking place during cataract surgery

Sponsors

Prim. Prof. Dr. Oliver Findl, MBA
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 105 Years
Healthy volunteers
No

Inclusion criteria

* Age-related cataract. * Patients in the age group of 21 years and above. * Patients with uncomplicated cataract. * Patients without any relevant systemic or ocular morbidity. * Patients with well dilating pupils. * Written informed consent prior to any study specific action.

Exclusion criteria

* Patients with complicated cataract. * Patients having corneal pathology. * Patients with any form of ocular inflammation. * Patients with glaucoma, retinal pathologies. * Patients with traumatic cataracts, subluxated and dislocated lens, prior h/o ocular surgery, pseudoexfoliation. * Any intraoperative complications like posterior capsule rupture. * In case of pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)

Design outcomes

Primary

MeasureTime frameDescription
Comparison between eye with capsular polishing and eye without capsular polishing concerning generation of posterior capsule opacification (PCO) in the same patient6 monthsPosterior capsule opacification will be graded using a score from 0 (clear capsule) to 10 (very severe PCO)

Secondary

MeasureTime frameDescription
Difference in the number of cells in the anterior chamber between the eye with capsular polishing and the eye without capsular polishing in the same patient6 monthsNumber of cells in the anterior chamber will be rated using a laser flare meter

Countries

Austria

Contacts

Primary ContactAndreea Fisus, MD
office@viros.at01 91021-57564
Backup ContactManuel Ruiß, MSc.
office@viros.at01 91021-57564

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026