Phacoemulsification Under Topical Anesthesia and Its Complications

The purpose of this study is to determine if topical anesthesia is safe for phacoemulsification in eyes with comorbidities.

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Key information

Conditions

Phacoemulsification

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

patients with cataract with a visual acuity less than 0.8

Exclusion criteria

none

Treatment and study plan

phacoemulsification

Procedure

Phacoemulsification under topical anesthesia

Primary outcomes

Number of Postoperative events

Time frame: 12 months

To describe any postoperatives events in a phacoemulsification surgery under topical anesthesia

Sponsors and collaborators

Lead sponsor

Instituto de Oftalmologia Ivo Correa-Meyer

Other

Registry information

Important dates

Study start: 2006
Primary completion: 2011
Study completion: 2011
First posted: Jun 27, 2011
Registry last updated: Jun 27, 2011

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