Cataract
Conditions
Keywords
Cataract, Cataract surgery, Phacoemulsification platform
Brief summary
Clinical performance of phacoemulsification platform Stellaris Elite with standard irrigation fluid bottles in myopic eyes. Anterior chamber depth and patients comfort will be compared between the two groups.
Detailed description
Today phacoemulsification is the most important and safest procedure to perform cataract surgery. However, there are factors that can increase the risk of complications, one of them is an intraoperative increase of intraocular pressure (IOP) which may cause choroidal haemorrhage, capsular block syndrome, or posterior capsular rupture . Also, more regularly, alterations of IOP provoke sudden changes of the anterior chamber depth, especially in myopic eyes due to intra-operative inverse irido-capsular block, which may result in pain or discomfort for the patient. The deepening of the chamber also makes the surgical maneuvers more challenging in such eyes. As prevention of such adverse events, it is important to maintain a more or less constant IOP intraoperatively. To ensure this, the pressure of the irrigation fluid must be adjusted to the outflow of aqueous humor, usually by adapting the height of the irrigation fluid bottle (passive fluidics system). As a variable vacuum is produced at the phaco tip to enable the suction of lens fragments, there often are fluctuations of IOP, therefore the surgeon is required to constantly adjust the height of the irrigation fluid bottle. A novel method to relieve the surgeon of this often-distracting task is to use all-in-one phacoemulsification systems that are able to monitor vacuum flow rates and then adjust the pressure of the irrigation fluid intraoperatively, also resulting in less fluctuations of IOP (active fluidics system). This should also result in reduced deepening of the anterior chamber and less risk of the adverse events as explained above.
Interventions
DEVICEStellaris Elite
The Stellaris and the Stellaris Elite platform will be used in myopic patients (axial length \> 25.0 mm) during cataract surgery
Sponsors
Prim. Prof. Dr. Oliver Findl, MBA
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to 105 Years
Healthy volunteers
No
Inclusion criteria
* Age-related cataract in both eyes * Scheduled for bilateral cataract surgery * Myopic patiens with axial eye length \>25.0mm * Age 21 and older * Written informed consent prior to recruitment
Exclusion criteria
* Pregnancy (pregnancy test will be taken pre-operatively in women of reproductive age) * Preceded ophthalmic surgery * Any ophthalmic abnormality that could compromise the measurements * Concurrent participation in another drug or device clinical investigation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Anterior chamber depth | 12 months | Anterior chamber depth will be measured using the IOL Master 700. Fluctuations in anterior chamber depth will be compared between the eyes where Stellaris and the contralateral eyes in which the Stellaris Elite platform was used |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patients discomfort | 12 months | Patients will be asked concerning their discomfort during both cataract surgeries and results will be recorded using an visual analogue scale. In the visual analogue scale 10 means highest discomfort and 1 stands for lowest discomfort. |
Countries
Austria
Contacts
Primary ContactKristina Stjepanek, MD
Backup ContactJulius Hienert, MD
Outcome results
None listed