Cycloplegic Delivery Investigation

The Ohio State University

Status: Completed

Conditions: Healthy

Treatments: Procedure: Mydriasis/cycloplegia via different modes of administration

Study type: Interventional

Funder types: Other

Identifiers

NCT00472524

2003H0072

Details and patient eligibility

About

The goal of this study is to compare the effectiveness of the administration of sequential drops, a combination drop and a combination spray for producing mydriasis and cycloplegia.

Sex: All

Ages: 8 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• patients ages 8 to 30 with best corrected acuity of 20/30 or better in both eyes at distance and near will be recruited.

Exclusion criteria

• vision not correctable to 20/30 or better

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)