Viewing Study NCT03761758


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Study NCT ID: NCT03761758
Status: COMPLETED
Last Update Posted: 2018-12-03
First Post: 2018-11-29
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Tolerability of a Novel Spectacle Design With Reduced Peripheral Contrast
Sponsor: SightGlass Vision, Inc.
Organization:

Study Overview

Official Title: Tolerability of a Novel Spectacle Design With Reduced Peripheral Contrast
Status: COMPLETED
Status Verified Date: 2018-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: WALNUT
Brief Summary: Prospective, randomized, subject-masked 3-arm clinical study to assess the pediatric acceptability across three iterations of a novel spectacle lens design.
Detailed Description: This feasibility study was conducted to assess the performance of three experimental spectacle lens designs (spectacle lenses) in children between 6 and 9 years of age with myopia.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: True
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: