Terminated PHASE3 INTERVENTIONAL 2-arm NCT00425464

A Prospective Multicenter Clinical Study to Evaluate the Safety and Effectiveness of the Synchrony Dual Optic Intraocular Lens in Patients Undergoing Cataract Extraction

Sponsor: Abbott Medical Optics

Conditions Cataract

Interventions Standard Monofocal Intraocular Lens Synchrony® Dual Optic Intraocular Lens

Updated 7 times since 2017 Last updated: Sep 16, 2013 Started: Nov 30, 2005 Primary completion: Apr 30, 2013 Completion: Apr 30, 2013

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

This trial was terminated. No reason was provided.

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A PHASE3 clinical study on Cataract, this trial is terminated or withdrawn. The trial is conducted by Abbott Medical Optics and has accumulated 7 data snapshots since 2005. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

7 versions recorded

Sep 2024 — Present [monthly]

Terminated PHASE3
Jul 2024 — Sep 2024 [monthly]

Terminated PHASE3
Apr 2022 — Jul 2024 [monthly]

Terminated PHASE3
Jan 2021 — Apr 2022 [monthly]

Terminated PHASE3
Jun 2018 — Jan 2021 [monthly]

Terminated PHASE3

▶ Show 2 earlier versions

Feb 2017 — Jun 2018 [monthly]

Terminated PHASE3
Jan 2017 — Feb 2017 [monthly]

Terminated PHASE3

First recorded

Nov 2005

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Abbott Medical Optics

Data source: Abbott Medical Optics

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

Alexandria, United States , Bloomington, United States , Boynton Beach, United States , Chesterfield, United States , Des Plaines, United States , Eugene, United States , Glenview, United States , Honolulu, United States , Houston, United States , Laguna Hills, United States and 10 more locations