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A Prospective Study To Evaluate The Raindrop Near Vision Inlay In Presybopic or Pseudophakic Patients Treated With Mitomycin C Following Femtosecond Flap Creation.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03101501
Recruitment Status : Terminated (The manufacturing company of the Raindrop Corneal Inlay has stopped distribution or sales of the product.)
First Posted : April 5, 2017
Last Update Posted : August 13, 2019
Sponsor:
Information provided by (Responsible Party):
Jeffrey Whitman, MD, Key-Whitman Eye Center

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Terminated
Actual Primary Completion Date : February 1, 2018
Actual Study Completion Date : February 1, 2018