NCT07025707 Comparison of Two Different Methods for Calculating Intraocular Lens Tilt and Decentration
| NCT ID | NCT07025707 |
| Status | Recruiting |
| Phase | — |
| Sponsor | St John of God Hospital, Vienna |
| Condition | Intraocular Lens |
| Study Type | OBSERVATIONAL |
| Enrollment | 15 participants |
| Start Date | 2025-07-01 |
| Primary Completion | 2025-08-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 15 participants in total. It began in 2025-07-01 with a primary completion date of 2025-08-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Agreement and Reproducibility of Intraocular Lens Tilt and Decentration Measurements: A Comparison between CASIA2 and CILT
Eligibility Criteria
Inclusion Criteria: * planned cataract surgery * agreement to participation Exclusion Criteria: * Zonulolysis * Strabismus * Reduced Compliance * Axial length \<20 or \>25 mm * Keratokonus * PEX
Contact & Investigator
Michael Amon, Prim. Univ. Prof. Dr.
STUDY CHAIR
Hospital St. John of God
Frequently Asked Questions
Who can join the NCT07025707 clinical trial?
This trial is open to participants of all sexes, aged 21 Years or older, studying Intraocular Lens. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07025707 currently recruiting?
Yes, NCT07025707 is actively recruiting participants. Contact the research team at konstantin.seiller@gmail.com for enrollment information.
Where is the NCT07025707 trial being conducted?
This trial is being conducted at Vienna, Austria.
Who is sponsoring the NCT07025707 clinical trial?
NCT07025707 is sponsored by St John of God Hospital, Vienna. The principal investigator is Michael Amon, Prim. Univ. Prof. Dr. at Hospital St. John of God. The trial plans to enroll 15 participants.