In-vivo Behavior of Asqelio Monofocal Biaspheric Intraocular Lens

NCT04971863 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2024-01-31

No results posted yet for this study

Summary

This is a study to evaluate the 24 month postoperative incidence and intensity of posterior capsular opacity in patients submitted to cataract surgery and implanted with a hydrophobic monofocal IOL.

Conditions

  • Cataract
  • Intraocular Lens Complication

Sponsors & Collaborators

  • Hospital Universitario La Fe

    collaborator OTHER
  • AST Products, Inc.

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-30
Primary Completion
2023-10-31
Completion
2024-01-05

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 NCT04971863 on ClinicalTrials.gov