Cycloplegic Delivery Investigation

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00472524

Enrollment

Registered

2007-05-11

Start date

Unknown

Completion date

Unknown

Last updated

2008-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

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.

Interventions

PROCEDUREMydriasis/cycloplegia via different modes of administration

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

8 Years to 30 Years

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026