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COMPLETED Phase 4

Evaluation of Effective Lens Position With a Uniplanar Bi-aspheric IOL

NCT01248572 · View on ClinicalTrials.gov ↗

Study Summary

The primary goal of this study is to determine the effective lens position (ELP) - or location an intraocular lens (IOL) "sits" in the eye - of the Softec HD IOL. A secondary study goal is to determine if measures of the eye taken prior to surgery can reliably predict postoperative ELP.

Conditions Studied

Interventions

  • DEVICE Softec HD IOL

Study Locations (3)

Arizona

  • Barnet-Dulaney-Perkins Eye Center — Phoenix

Florida

  • Eye Centers of Florida — Fort Myers

Georgia

  • Harbin Clinic — Rome

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2010-10
Est. Completion 2012-03
Phase Phase 4

Sponsor

Lenstec Incorporated

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01248572

The ClinicalTrials.gov registry entry for NCT01248572 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 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lenstec Incorporated, which has 1 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 Cataract appearing as the primary indexed condition, and to 1 intervention — of which Softec HD 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: NCT01248572 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Arizona, Florida, Georgia. 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 NCT01248572 about?

NCT01248572 is a clinical study titled "Evaluation of Effective Lens Position With a Uniplanar Bi-aspheric IOL". The primary goal of this study is to determine the effective lens position (ELP) - or location an intraocular lens (IOL) "sits" in the eye - of the Softec HD IOL. A secondary study goal is to determine if measures of the eye taken prior to surgery can reliably predict postoperative ELP.

What is the current status of trial NCT01248572?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2010-10. Estimated completion is 2012-03.

What conditions does trial NCT01248572 study?

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

What interventions are being tested in trial NCT01248572?

The interventions under investigation include: Softec HD IOL (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01248572?

This trial is sponsored by Lenstec Incorporated, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01248572 being conducted?

This trial has 3 study locations across Arizona, Florida, Georgia. 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