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A Study Comparing Two Monofocal, Aspheric, Hydrophobic Acrylic Intraocular Lenses: the Alcon CLAREON® and the Abbott Medical Optics PCB00

NCT03364972 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 145

Last updated 2019-08-06

No results posted yet for this study

Summary

This is a bilateral randomised controlled study to compare visual performance, refractive outcome, forward light scatter, patient satisfaction and objective measurement of glistenings following insertion of two monofocal, aspheric, hydrophobic acrylic intraocular lenses (IOLs). A new product is compared with an established one.

Conditions

  • Cataract Extraction
  • Phacoemulsification
  • Glistenings
  • Intraocular Lens Implant
  • Hydrophobic Acrylic
  • Cataract Surgery
  • Light Scatter
  • Patient Satisfaction
  • Patient Related Outcome Measures

Interventions

DEVICE

Cataract surgery

Conventional small-incision phacoemulsification cataract surgery with insertion of intraocular lens implant

Sponsors & Collaborators

  • City, University of London

    collaborator OTHER

  • King's College London

    collaborator OTHER

  • Guy's and St Thomas' NHS Foundation Trust

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-02-06
Primary Completion
2019-08-01
Completion
2019-08-01

Countries

  • United Kingdom

Study Locations

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Entities

Companies

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 NCT03364972 on ClinicalTrials.gov