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Clinical trial

Use of the VisuMax™ Femtosecond Laser Lenticule Removal Procedure for the Correction of Myopia

NCT01638390 is registered in ClinicalTrials.gov with Carl Zeiss Meditec, Inc. as lead sponsor.

NCT NCT01638390
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Registry record

As filed in ClinicalTrials.gov.

Title
Use of the VisuMax™ Femtosecond Laser Lenticule Removal Procedure for the Correction of Myopia
Lead sponsor
Carl Zeiss Meditec, Inc.
Phase
Phase 1
Overall status
Completed
Start date
July 31, 2012
Completion date
April 30, 2016
Enrollment
357 (actual)
Sites
5

Conditions

As the registry lists them; a condition with its own page is linked.

myopia