Viewing Study NCT06636708



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06636708
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-08

Brief Title: Efficacy of Nanodropper-mediated Topical Anesthetic
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of Nanodropper-mediated Microdrops Vs Standard Drops of 05 Proparacaine HCl
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to compare the onset and duration of numbness of the surface of the eye following the administration of numbing drops called proparacaine using either a standard eye drop bottle or a Nanodropper adaptor The Nanodropper is designed to administer smaller-sized drops or microdrops

Participants will

1 Complete a baseline eye exam
2 Receive a numbing drop using a standard dropper in one eye and the Nanodropper in the other eye
3 Have their eyes tested for numbness at specific time points 30 seconds 1 2 5 and 10 minutes after getting the drops
4 Tell the researchers if they feel pain during the eye sensation tests
5 Complete a survey about their experience with the eyedrops and testing procedure

This study could help us find a way to use less medication while still effectively administering eye medications potentially saving money and reducing medical waste
Detailed Description: None

Study Oversight

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