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Registry Study on Intraocular Lenses Manufactured by Teleon Surgical B.V.

NCT05290870 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2183

Last updated 2024-07-03

No results posted yet for this study

Summary

This is a retrospective, observational (Registry) study aiming to collect safety and performance data on the use of intraocular lenses (IOLs) manufactured by Teleon Surgical B.V. according to routine practice.

Conditions

  • Aphakia
  • Cataract
  • Clear Lens Exchange
  • Refractive Lens Exchange

Interventions

DEVICE

Posterior-chamber intraocular lens

Implantation of a posterior-chamber intraocular lens to correct aphakia after removal of the crystalline lens

Sponsors & Collaborators

  • MaganaMed GmbH

    collaborator UNKNOWN

  • Teleon Surgical B.V.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-01
Primary Completion
2024-02-29
Completion
2024-04-30

Countries

  • Netherlands

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 NCT05290870 on ClinicalTrials.gov