Evaluation of the Rotational Stability

NCT03247751 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 95

Last updated 2023-06-07

No results posted yet for this study

Summary

To evaluate rotational stability of the investigational device implanted after cataract surgery.

Conditions

  • Cataract

Interventions

DEVICE

intraocular lens

Implant NIDEK intraocular lens after cataract surgery

Sponsors & Collaborators

  • Nidek Co. LTD.

    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
2016-06-30
Primary Completion
2017-08-31
Completion
2017-11-30

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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 NCT03247751 on ClinicalTrials.gov