Viewing Study NCT05265910



Ignite Creation Date: 2024-05-06 @ 5:19 PM
Last Modification Date: 2024-10-26 @ 2:26 PM
Study NCT ID: NCT05265910
Status: COMPLETED
Last Update Posted: 2022-05-03
First Post: 2021-12-14

Brief Title: A Study Comparing the Efficacy of Pataday Once Daily Relief Extra Strength to Claritin Tablets 24-Hour in Subjects With Allergic Conjunctivitis
Sponsor: Andover Research Eye Institute
Organization: Andover Research Eye Institute

Study Overview

Official Title: A Single-Center Randomized Double-Masked Parallel Study Comparing the Efficacy of Pataday Once Daily Relief Extra Strength to Claritin Tablets 24-Hour in Reducing Ocular Itching in Subjects With Allergic Conjunctivitis
Status: COMPLETED
Status Verified Date: 2022-03
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: None
Brief Summary: This is a single-center randomized double-masked parallel study In this clinical study the efficacy comparison between Pataday Once Daily Relief Extra Strength and Claritin Tablets 24-Hour will be made using the Ora-CAC model a validated clinical model accepted by regulatory agents for assessing the efficacy of products on the signs and symptoms of allergic conjunctivitis
Detailed Description: None

Study Oversight

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