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Clinical Analysis of Ocular Parameters Contributing to Intraoperative Pain During Standard Phacoemulsification | Clinical Trials | Clareo Health

COMPLETED

Clinical Analysis of Ocular Parameters Contributing to Intraoperative Pain During Standard Phacoemulsification

NCT03031652•Kyungpook National University Hospital

View on ClinicalTrials.gov

Summary

Charts of 142 patients who underwent standard phacoemulsification under topical anesthesia between March and August 2016 were reviewed. The pain during phacoemulsification and 1 h after surgery was assessed and compared using a visual analog scale.

Detailed Description

Patients scheduled for elective phacoemulsification and intraocular lens implantation with the Infiniti Vision System (Alcon, Fort Worth, USA) were included. All operations were performed in Kyungpook National University Hospital by the same surgeon between March and August 2016.

Eligibility

Age

All ages

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Patients underwent phacoemulsification with topical anesthesia

Exclusion Criteria

•Patients who needed general anesthesia or were taking medications capable of affecting perceived pain
•Patients who had traumatic cataract and/or conditions likely to require vitrectomy and trans-scleral fixation of posterior chamber intraocular lens

Locations (1)

Kyungpook national university hospital

Daegu, Samduk-2ga, Jung-gu, South Korea

Key Dates

Start Date

March 1, 2016

Primary Completion Date

August 31, 2016

Completion Date

December 31, 2016

Last Updated

January 25, 2017

Enrollment

142

ACTUAL participants

Conditions

Phacoemulsification

Interventions

Phacoemulsification

DEVICE

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

NCT03761745

Intraocular Lens ComplicationPhacoemulsification

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SUSPENDEDPHASE3

Intracameral Antibiotic Safety Study

NCT02590523

Intracameral AntibioticsCataract Surgery+4 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 25, 2017Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Clinical Analysis of Ocular Parameters Contributing to Intraoperative Pain During Standard Phacoemulsification

Inclusion Criteria

Exclusion Criteria

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Intracameral Antibiotic Safety Study

Correlation Between Postoperative Central Corneal Thickness and Endothelial Damage After Cataract Surgery

Efficacy and Safety of PRO-155 Versus Nevanac in Post Phacoemulsification