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India PanOptix Post Marketing Study

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Status

Completed

Conditions

Cataract

Treatments

Procedure: Cataract surgery
Device: Acrysof IQ PanOptix IOL

Study type

Observational

Funder types

Industry

Identifiers

NCT03706066
ILD432-P001
CTRI/2018/11/016467 (Other Identifier)

Details and patient eligibility

About

The purpose of this Post Marketing Study is to study the safety and effectiveness of the ACRYSOF IQ PanOptix intraocular lens (IOL) in an Indian population.

Full description

The study population will consist of adult Indian males and females, at least 18 years of age or older at the time of screening, with no ocular pathology that could confound study outcomes, who are advised bilateral cataract extraction and who desire an IOL that provides the potential for correction of near, intermediate, and distance vision. Both eyes will be implanted. The second eye surgery will take place 15-30 days after the first eye surgery. Subjects will be followed for approximately 3 months after the second eye surgery. Total individual subject participation will be approximately 4 months. This study will be conducted in India.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Able to comprehend and willing to sign informed consent and complete all required postoperative follow-up procedures;
  • Advised cataract extraction in both eyes and agreed for bilateral implantation of ACRYSOF IQ PanOptix lens;
  • Preoperative regular keratometric astigmatism of ≤1.0 D in both eyes.

Exclusion criteria

  • Pregnant or lactating, current or planned, during the course of the study;
  • Retinal abnormalities (Macular Degeneration, dystrophy, edema , traction or other pathologies affecting vision);
  • Clinically significant corneal abnormalities;
  • History of retinal conditions;
  • Previous refractive surgery, including LASIK;
  • Glaucoma;
  • Any condition that may not be appropriate to this study, as per the Investigator's expert medical opinion.

Other protocol-specified inclusion and/or exclusion criteria may apply.

Trial design

80 participants in 1 patient group

PanOptix
Description:
Cataract surgery with implantation of Acrysof IQ PanOptix IOL
Treatment:
Device: Acrysof IQ PanOptix IOL
Procedure: Cataract surgery

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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