Cycloplegic Delivery Investigation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00472524
Recruitment Status : Completed
First Posted : May 11, 2007
Last Update Posted : July 3, 2008
Information provided by:
Ohio State University

Brief 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.

Condition or disease Intervention/treatment Phase
Healthy Procedure: Mydriasis/cycloplegia via different modes of administration Not Applicable

Study Type : Interventional  (Clinical Trial)
Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic

Information from the National Library of Medicine

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Ages Eligible for Study:   8 Years to 30 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00472524

Sponsors and Collaborators
Ohio State University
Principal Investigator: Marjean Kulp, OD, MS Ohio State University Identifier: NCT00472524     History of Changes
Other Study ID Numbers: 2003H0072
First Posted: May 11, 2007    Key Record Dates
Last Update Posted: July 3, 2008
Last Verified: July 2008