Preoperative Cataract Pupillary Dilation: Inpatient At The Ambulatory Surgery Center vs Outpatient Dilation Prior To Arrival At The Ambulatory Surgery Center

This study was done to compare efficacy, safety and efficiencies of various methods of pupil dilation prior to cataract surgery.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Pupil Dilation Prior to Cataract Surgery In-patient Eye Diseases Mydriasis Pupil Dilation Prior to Cataract Surgery Out-patient Pupil Disorders

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Ability to self administer eye or have a helper for the task of administering eye drops.
Ability to follow and eye drop administration schedule.
No noted ocular abnormalities.
Bilateral cataract surgery anticipated.

Exclusion criteria

Inability to self administer eye drops or have assistance with eye drop administration.
Health problems that would contraindicate self administration of dilating eye drops such as poor cardiovascular or respiratory status.

Treatment and study plan

Pupil dilation with phenylephrine 10% vs cyclopentolate 2%

Other

Sponsors and collaborators

Lead sponsor

Northwest Kansas Surgery Center

Other

Registry information

Official study title

Preoperative Cataract Pupillary Dilation: Inpatient vs Outpatient

Important dates

Study start: 2007
Primary completion: 2008
Study completion: 2008
First posted: Jul 26, 2010
Registry last updated: Jul 26, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed