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Comparing an Intraoperative vs. a Standard Wavefront Device

NCT03749798 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-11-23

No results posted yet for this study

Summary

Comparison of intraoperative measured wavefront data with pre- and post-operative wavefront data.

Conditions

  • Cataract

Interventions

PROCEDURE

Cataract surgery

Intraoperative wavefront measurements will be carried out during cataract surgery

Sponsors & Collaborators

  • Prim. Prof. Dr. Oliver Findl, MBA

    lead OTHER

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
105 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-01
Primary Completion
2019-12-01
Completion
2019-12-01

Countries

  • Austria

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 NCT03749798 on ClinicalTrials.gov