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Intraocular Lens Power Calculation for Combined Phaco-vitrectomy Procedures

C

Cantonal Hospital of St. Gallen

Status

Unknown

Conditions

Combined Phaco-vitrectomy
Intraocular Lens Calculation

Treatments

Diagnostic Test: Biometry

Study type

Observational

Funder types

Other

Identifiers

NCT03856346
Phaco-vity-biometry study

Details and patient eligibility

About

The aim of the study is to evaluate the degree of refractive error postoperatively in combined procedures and to calculate a new constant in order to improve current state of the art biometry calculations.

Full description

The IOL power calculation in combined phaco-vitrectomy has been performed similar to that in cataract surgery alone. In patients who undergo combined phaco-vitrectomy, deviations in refractive outcomes may be observed because of possible errors in measurement of axial length, changes in the properties of the vitreous cavity after removal of the vitreous, or intraocular tamponade. Most of the previous studies have reported variable degrees of myopic shift after phaco-vitrectomy for diabetic retinopathy, epiretinal membrane, and macular hole. Furthermore, use of intraoperative gas may increase further the risk of anterior displacement of the intraocular lens which may induce a higher myopic shift. However, these publications did not provide any quantification of the spherical deviations nor calculate any specific constant in order to improve currents state of art biometry calculations.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who undergo a combined procedure with phacoemulsification and pars plana vitrectomy

Exclusion criteria

  • Sulcus fixation of the IOL, sulcus suture of the IOL, or intra-scleral IOL fixation because of intraoperative posterior capsule rupture
  • corneal disease, such as keratoconus, that interfered with refractive results
  • IOL implantation with a toric IOL or multifocal IOL
  • History of previous vitrectomy or corneal transplantation
  • Other coexisting ocular disease such as proliferative diabetic retinopathy, advanced age-related macular degeneration, uveitis, acute retinal necrosis, Coat's disease, proliferative vitreous retinopathy, or trauma
  • Intraocular tamponade using silicon oil

Trial design

200 participants in 1 patient group

Phaco-vitrectomy
Treatment:
Diagnostic Test: Biometry

Trial contacts and locations

1

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Central trial contact

Josef Guber, MD

Data sourced from clinicaltrials.gov

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