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临床试验

Lacrima VR for Dry Eye Disease and Meibomian Gland Dysfunction

NCT:NCT07415330 · NOT_YET_RECRUITING

NCT编号NCT07415330
状态NOT_YET_RECRUITING
开始日期2026-07-20
完成时间2026-09-01
SponsorDemaod Ltd (INDUSTRY)
First posted
Last updated

简要摘要

This is a prospective, multi-center, randomized, sham-controlled clinical investigation designed to evaluate the safety and effectiveness of the Lacrima VR system in adult subjects with Dry Eye Disease (DED) and Meibomian Gland Dysfunction (MGD). Subjects will be randomized in a 1:1 ratio to receive either active Lacrima VR treatment or a sham device with reduced luminance. Effectiveness will be assessed primarily by change in Tear Break-Up Time (TBUT), and safety will be evaluated by the incidence of device-related adverse events.

官方来源

在 ClinicalTrials.gov 上查看 →

数据来自 ClinicalTrials.gov API。有关最新状态,请参阅官方记录。

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