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NCT01292629 · ClinicalTrials.gov registry record · NA
Comparison of the Hoya Surgical Optics (HSO) iSert 251 Posterior Chamber Aspheric Aphakic Intraocular Lens to Historical / Literature Controls.
A NA study of Cataract and Aphakia, sponsored by Hoya Surgical Optics.
- Completed
- Registry status
- NA
- Development phase
- 125
- Enrollment target
- 5
- Study locations
NCT01292629 is a NA study of Cataract and Aphakia that has completed, run by Hoya Surgical Optics. The registered enrollment target is 125 participants, below the 227-participant average among 83 other Cataract trials with a reported enrollment target (45% lower). The trial reports 5 study locations across 4 states.
The verdict
NCT01292629, a NA study of Cataract and Aphakia, has completed, sponsored by Hoya Surgical Optics.
- COMPLETED
- Registry status
- NA
- Development phase
- 125 participants
- Enrollment target
- 5
- Study locations
Study Summary
The purpose of this multi-center clinical trail is to determine the safety and efficacy of the iSert 251 for the correction of aphakia.
Interventions
- DEVICE iSert 251 intraocular lens
Study Locations (5)
Florida
- Katzen Eye Care and Laser Center - Boynton Beach
- Center for Excellence in Eye Care - Miami
Arizona
- Schwartz Laser Eye Center - E. Shea Blvd, Suite C101
Indiana
- Eye Surgeons of Indiana - Indianapolis
Massachusetts
- Eye Health Vision Centers - North Dartmouth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 125 participants |
| Start Date | 2011-02 |
| Est. Completion | 2012-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01292629
The ClinicalTrials.gov registry entry for NCT01292629 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 125 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 227-participant average among 83 other Cataract trials with a reported enrollment target (45% lower). The listed sponsor is Hoya Surgical Optics, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cataract appearing as the primary indexed condition, and to 1 intervention - of which iSert 251 intraocular lens is the first listed.
NCT01292629 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Florida, Arizona, Indiana.
Frequently Asked Questions
What is clinical trial NCT01292629 about?
NCT01292629 is a clinical study titled "Comparison of the Hoya Surgical Optics (HSO) iSert 251 Posterior Chamber Aspheric Aphakic Intraocular Lens to Historical / Literature Controls.". The purpose of this multi-center clinical trail is to determine the safety and efficacy of the iSert 251 for the correction of aphakia.
What is the current status of trial NCT01292629?
This trial is currently completed. It is a NA study. The enrollment target is 125 participants. The study started on 2011-02. Estimated completion is 2012-05.
What conditions does trial NCT01292629 study?
This clinical trial studies the following conditions: Cataract, Aphakia.
What interventions are being tested in trial NCT01292629?
The interventions under investigation include: iSert 251 intraocular lens (DEVICE).
Who is sponsoring clinical trial NCT01292629?
This trial is sponsored by Hoya Surgical Optics, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01292629 being conducted?
This trial has 5 study locations across Arizona, Florida, Indiana, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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