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COMPLETED Phase 4

Visual Function After Bilateral Implantation of AcrySof® Toric

NCT00758550 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.

Conditions Studied

Interventions

  • DEVICE AcrySof® Toric IOL
  • DEVICE AcrySof Natural

Study Locations (1)

Texas

  • Alcon Call Center — Fort Worth

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2007-04
Phase Phase 4

Sponsor

Alcon Research

111 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00758550

The ClinicalTrials.gov registry entry for NCT00758550 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 111 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Visual Function appearing as the primary indexed condition, and to 2 interventions — of which AcrySof® Toric IOL is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00758550 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00758550 about?

NCT00758550 is a clinical study titled "Visual Function After Bilateral Implantation of AcrySof® Toric". The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.

What is the current status of trial NCT00758550?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2007-04.

What conditions does trial NCT00758550 study?

This clinical trial studies the following conditions: Visual Function. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00758550?

The interventions under investigation include: AcrySof® Toric IOL (DEVICE), AcrySof Natural (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00758550?

This trial is sponsored by Alcon Research, which has 111 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00758550 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial