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

NCT03031652 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 142

Last updated 2017-01-25

No results posted yet for this study

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.

Conditions

  • Phacoemulsification

Interventions

DEVICE

Phacoemulsification

The device device used to provide and perform small profile entry for cataract extraction with or without option of insertion of a specified intraocular lens implant

Sponsors & Collaborators

  • Kyungpook National University Hospital

    lead OTHER

Principal Investigators

  • Hong Kyun Kim, M.D.,Ph.D. · Department of ophthalmology, Kyungpook national university hospital

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-01
Primary Completion
2016-08-31
Completion
2016-12-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03031652 on ClinicalTrials.gov