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Comparison of Two Phacoemulsification-methods: EasyTip 2.2mm vs. Infusion Assisted EasyTip 2.2mm

Comparison of Two Phacoemulsification-methods: EasyTip 2.2mm vs. Infusion Assisted EasyTip 2.2mm

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01936727
Enrollment
50
Registered
2013-09-06
Start date
2011-12-31
Completion date
2012-08-31
Last updated
2013-09-06

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

Conditions

Cataracts

Keywords

efficiency and safety

Brief summary

The aim of this study was to compare the intraoperative efficiency, safety and postoperative outcomes of cataract surgery with two different high-fluidic settings.

Interventions

PROCEDUREcataract surgery

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* bilateral age-related cataract * good overall physical constitution * LOCS 2-5

Exclusion criteria

* previous intraocular surgery or ocular trauma * previous corneal pathology * previous endothelial cell count \<1200 * glaucoma * uveitis * PEX * diabetic retinopathy and any other severe retinal pathology that would make a postoperative visual acuity of 20/40 (decimal equivalent = 0.5) or better unlikely * intraocular complication like posterior capsular * postoperative comlpications (e.g. postoperative uveitis)

Design outcomes

Primary

MeasureTime frameDescription
phacoemulsification timeintraoperativetime spent for the phacoemulsification process was the phacoemulsification tip time (PTT) needed to divide the nucleus and the PTT needed to conquer it
effective phacoemulsification timeintraoperativtime in seconds required had 100% power been used throughout the phacoemulsification process documented for the separation of the nucleus (divide) and the aspiration of the quadrants (conquer)
fluid volumeintraoperativamount of BSS used for dividing and conquering

Secondary

MeasureTime frameDescription
postoperative corneal oedema1 day, 1 week, 6 monthscentral corneal thickness
postoperative endotheial cell loss6 months

Countries

Austria

Outcome results

None listed

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