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NCT03612284

Scleral Contact Lens Insertion Solution Study

Completed NA Last updated 18 January 2019
What this trial tests

NA trial testing contact lens insertion solution in Irregular; Contour of Cornea in 30 participants. Completed in 30 November 2018.

Timeline
27 November 2017
Primary endpoint
30 November 2018
30 November 2018

Quick facts

Lead sponsorJennifer Fogt
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment30
Start date27 November 2017
Primary completion30 November 2018
Estimated completion30 November 2018
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Jennifer Fogt

Who can join

18 and older, any sex, with Irregular; Contour of Cornea. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the clinical ocular compatibility (feasibility of safety and efficacy) of a patented solution (US Patent 2,259,437, Stone) which contains multiple essential ions and has a pH and tonicity which more closely mimics human tears as compared to the subjects' current habitual scleral lens insertion solution.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Jennifer Fogt trials

Trials by the same sponsor.

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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/NCT03612284.

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