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Comparative Clinical Study of Intraocular Lens Injectors Lioli™, Pioli™, and Pioli™ Plus

NCT07140029 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2025-08-24

No results posted yet for this study

Summary

The goal of this observational study is to evaluate whether different intraocular lens (IOL) injectors affect surgical outcomes in patients aged 40 and older undergoing cataract surgery. The main questions it aims to answer are:

* Do different IOL injectors change the size of the corneal incision during surgery?
* Do the injectors lead to different rates of complications during or after surgery? Researchers will compare the use of three different IOL injectors: two preloaded models (pioli™ and pioli™ Plus) and one manually loaded model (lioli™), to see if the preloaded systems improve surgical results compared to the manual one.

Participants will:

* Undergo routine cataract surgery using one of the three injectors, randomly assigned.
* Have measurements taken before and after surgery (e.g., vision tests, corneal incision size).
* Be monitored for any side effects or complications during and after the procedure.

Conditions

  • Cataract
  • Lens Implantation, Intraocular

Sponsors & Collaborators

  • AST Products, Inc.

    lead INDUSTRY

Principal Investigators

  • Adrián Hernández Martínez, MD, PhD · OftalVist Sevilla

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-31
Primary Completion
2025-11-30
Completion
2025-12-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07140029 on ClinicalTrials.gov