Skip to content

Corneal Biomechanics and Surgically Induced Astigmatism in Pseudoexfoliation Syndrome

Influence of Corneal Biomechanics on Surgically Induced Astigmatism After Cataract Surgery in Patients With Pseudoexfoliation Syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07722247
Enrollment
70
Registered
2026-07-23
Start date
2026-07-20
Completion date
2026-10-01
Last updated
2026-08-18

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

Conditions

Pseudoexfoliation Syndrome, Cataract, Astigmatism

Keywords

corneal biomechanics, corneal hysteresis, corneal resistence factor, cataract surgery, pseudoexfoliation syndrome, surgically induced astigmatism

Brief summary

This prospective study aims to evaluate the influence of corneal biomechanical properties on surgically induced astigmatism following standard phacoemulsification cataract surgery in patients with pseudoexfoliation syndrome compared with patients without pseudoexfoliation. Corneal hysteresis (CH), corneal resistance factor (CRF) and corneal astigmatism will be measured before surgery and at postoperative follow-up visits. The relationship between changes in corneal biomechanics and surgically induced astigmatism will be analyzed.

Detailed description

Pseudoexfoliation syndrome is associated with structural alterations of the anterior segment and may affect the biomechanical behavior of the cornea. Corneal hysteresis (CH) and corneal resistance factor (CRF), measured using the Ocular Response Analyzer, are indicators of corneal biomechanical properties and may influence the corneal response to cataract surgery and magnitude of surgically induced astigmatism. This prospective, single-center observational study will include approximately 70 patients undergoing routine phacoemulsification cataract surgery. Participants will be allocated into two groups according to the presence or absence of pseudoexfoliation syndrome. CH, CRF and corneal astigmatism will be measured preoperatively and postoperatively at scheduled follow-up visits at postoperative day 1, 7 and 30. Surgically induced astigmatism will be calculated from keratometric measurements. The primary objective of the study is to determine whether correlations exist between corneal biomechanical properties (CH and CRF) and surgically induced astigmatism in patients with pseudoexfoliation syndrome and to compare these correlations with those observed in patients without pseudoexfoliation syndrome.

Interventions

Standard phacoemulsification cataract surgery with intraocular lens implantation performed according to routine clinical practice.

Sponsors

Kata Culina
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 50-85 years * Age-related cataract scheduled for standard phacoemulsification cataract surgery with intraocular lens implantation * Presence of pseudoexfoliation syndrome (PEX group) or absence of pseudoexfoliation syndrome (control group) * Ability to provide written informed consent * Willingness to attend all scheduled postoperative follow-up visits

Exclusion criteria

* Previous ocular surgery in the study eye * Corneal diseases or abnormalities that may affect corneal biomechanical measurements or keratometry * Glaucoma and ocular hypertension * Ocular trauma or active ocular inflammation

Design outcomes

Primary

MeasureTime frameDescription
Correlation between corneal biomechanical properties and surgically induced astigmatismPreoperative, postoperative day 1, postoperative day 7, and postoperative day 30.To evaluate the correlation between corneal hysteresis (CH), corneal resistance factor (CRF), and surgically induced astigmatism (SIA) after phacoemulsification cataract surgery in patients with pseudoexfoliation syndrome and compare the findings with a control group.

Countries

Croatia

Contacts

CONTACTKata Culina, MD, PhD
kculina@yahoo.com+38598615556
CONTACTAndela Jukic, MD, PhD
andela.jukic@yahoo.com+385981733912

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026