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NCT00829751 · ClinicalTrials.gov registry record · NA
The Physiological Consequence of Silicone-hydrogel Care-solution Bio-incompatibility
A NA study, sponsored by Southern California College of Optometry at Marshall B. Ketchum University.
- Completed
- Registry status
- NA
- Development phase
- 26
- Enrollment target
NCT00829751 is a NA study that has completed, run by Southern California College of Optometry at Marshall B. Ketchum University. The registered enrollment target is 26 participants.
The verdict
NCT00829751, a NA study, has completed, sponsored by Southern California College of Optometry at Marshall B. Ketchum University.
- COMPLETED
- Registry status
- NA
- Development phase
- 26 participants
- Enrollment target
Study Summary
The purpose of this study is to more objectively evaluate potential lens-material/care solution bio-incompatibilities. We will do this by measuring corneal staining and the amount of fluorescein dye diffusion into the eye.
Interventions
- DEVICE PureVision lenses soaked in ReNu Multiplus
- DEVICE PureVision lenses soaked in OptiFree RePlenish
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2008-11 |
| Est. Completion | 2011-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00829751
The ClinicalTrials.gov registry entry for NCT00829751 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Southern California College of Optometry at Marshall B. Ketchum University, which has 18 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which PureVision lenses soaked in ReNu Multiplus is the first listed.
NCT00829751 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00829751 about?
NCT00829751 is a clinical study titled "The Physiological Consequence of Silicone-hydrogel Care-solution Bio-incompatibility". The purpose of this study is to more objectively evaluate potential lens-material/care solution bio-incompatibilities. We will do this by measuring corneal staining and the amount of fluorescein dye diffusion into the eye.
What is the current status of trial NCT00829751?
This trial is currently completed. It is a NA study. The enrollment target is 26 participants. The study started on 2008-11. Estimated completion is 2011-06.
What interventions are being tested in trial NCT00829751?
The interventions under investigation include: PureVision lenses soaked in ReNu Multiplus (DEVICE), PureVision lenses soaked in OptiFree RePlenish (DEVICE).
Who is sponsoring clinical trial NCT00829751?
This trial is sponsored by Southern California College of Optometry at Marshall B. Ketchum University, which has 18 total clinical trials registered on ClinicalTrials.gov.
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