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Cycloplegic Delivery Investigation

NCT00472524 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2008-07-03

No results posted yet for this study

Summary

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.

Conditions

  • Healthy

Interventions

PROCEDURE

Mydriasis/cycloplegia via different modes of administration

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Marjean Kulp, OD, MS · Ohio State University

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
8 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00472524 on ClinicalTrials.gov