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A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice

Cataracts Clinical Trial

Official title:
A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice

Clinical Trial Summary

This is a post-market, prospective, randomized, multi-center, bilateral, open-label, cross-over, comparative clinical study. Study group will undergo preoperative LipiFlow treatment and Control group will not receive preoperative LipiFlow treatment. Three months postoperatively, both groups will be evaluated for clinical outcomes and the Control group will receive LipiFlow treatment as the cross-over group. The Control group will be evaluated at 4 months postoperative for clinical outcomes.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03708367
Study type Interventional
Source Johnson & Johnson Surgical Vision, Inc.
Contact
Status Completed
Phase N/A
Start date October 16, 2018
Completion date January 13, 2020
View Details
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