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NCT03691636

Eyelash Prostheses Compared to 5.0% Lifitegrast BID for Dry Eye Disease.

Status unknown NA Last updated 2 October 2018
What this trial tests

NA trial testing Eyelash prostheses in Dry Eye in 40 participants. Status unknown.

Timeline
2 October 2018
Primary endpoint
2 April 2019
1 May 2019

Quick facts

Lead sponsorD.E.L., LLC
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date2 October 2018
Primary completion2 April 2019
Estimated completion1 May 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

D.E.L., LLC

Who can join

50 and older, any sex, with Dry Eye. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a single-center, randomized, controlled trial to evaluate the safety and efficacy of eyelash prostheses versus 5.0% Lifitegrast BID, in 40 patients (20 randomized to each of two arms of the study) evaluated at 3 weeks and 5 weeks, respectively, after initiation of treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Dry Eye

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03691636.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing