Prospective Evaluation of an Hydrophilic Acrylic Intraocular Lens

NCT04907500 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 387

Last updated 2023-02-08

No results posted yet for this study

Summary

Evaluation of the clinical safety and effectiveness of an hydrophilic acrylic intraocular lens

Conditions

  • Cataract Senile

Interventions

DEVICE

Intraocular lens

Cataract surgery

Sponsors & Collaborators

  • Carl Zeiss Meditec AG

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-22
Primary Completion
2022-08-06
Completion
2022-12-16

Countries

  • Romania

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 NCT04907500 on ClinicalTrials.gov