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NCT02430428 · ClinicalTrials.gov registry record · NA

Correction of Myopia Wtih or Without Astigmatism Using the VisuMax™ Femtosecond Laser

A NA study of Myopia and Astigmatism, sponsored by Carl Zeiss Meditec.

Completed
Registry status
NA
Development phase
357
Enrollment target
5
Study locations

NCT02430428 is a NA study of Myopia and Astigmatism that has completed, run by Carl Zeiss Meditec. The registered enrollment target is 357 participants, above the 264-participant average among 90 other Myopia trials with a reported enrollment target (35% higher). The trial reports 5 study locations across 5 states.

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The verdict

NCT02430428, a NA study of Myopia and Astigmatism, has completed, sponsored by Carl Zeiss Meditec.

COMPLETED
Registry status
NA
Development phase
357 participants
Enrollment target
5
Study locations

Study Summary

The objective of this clinical trial is to evaluate the safety and effectiveness of the Carl Zeiss Meditec VisuMax™ Femtosecond Laser lenticule removal procedure for the reduction or elimination of myopia from ≥ -1.00 D to ≤ -10.00 D with ≤ -3.00 D cylinder (myopia with or without astigmatism) and MRSE ≤ -11.50 D.

Conditions Studied

Interventions

  • DEVICE Carl Zeiss Meditec VisuMax Femtosecond Laser

Study Locations (5)

Colorado

  • Dishler Laser Institute - Greenwood Village

Kansas

  • Discover Vision Centers - Leawood

South Dakota

  • Vance Thompson Vision - Sioux Falls

Texas

  • Slade and Baker Vision Center - Houston

Wisconsin

  • Davis Duehr Dean - Madison

Trial Details

FieldValue
Enrollment Target 357 participants
Start Date 2015-03
Est. Completion 2017-10
Phase NA

Sponsor

Carl Zeiss Meditec

18 total trials

What the Registry Record Tells You About NCT02430428

The ClinicalTrials.gov registry entry for NCT02430428 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 357 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 264-participant average among 90 other Myopia trials with a reported enrollment target (35% higher). The listed sponsor is Carl Zeiss Meditec, which has 18 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which Carl Zeiss Meditec VisuMax Femtosecond Laser is the first listed.

NCT02430428 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Colorado, Kansas, South Dakota.

Frequently Asked Questions

What is clinical trial NCT02430428 about?

NCT02430428 is a clinical study titled "Correction of Myopia Wtih or Without Astigmatism Using the VisuMax™ Femtosecond Laser". The objective of this clinical trial is to evaluate the safety and effectiveness of the Carl Zeiss Meditec VisuMax™ Femtosecond Laser lenticule removal procedure for the reduction or elimination of myopia from ≥ -1.00 D to ≤ -10.00 D with ≤ -3.00 D cylinder (myopia with or without astigmatism) and M...

What is the current status of trial NCT02430428?

This trial is currently completed. It is a NA study. The enrollment target is 357 participants. The study started on 2015-03. Estimated completion is 2017-10.

What conditions does trial NCT02430428 study?

This clinical trial studies the following conditions: Myopia, Astigmatism.

What interventions are being tested in trial NCT02430428?

The interventions under investigation include: Carl Zeiss Meditec VisuMax Femtosecond Laser (DEVICE).

Who is sponsoring clinical trial NCT02430428?

This trial is sponsored by Carl Zeiss Meditec, which has 18 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02430428 being conducted?

This trial has 5 study locations across Colorado, Kansas, South Dakota, Texas, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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