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NCT00597467 · ClinicalTrials.gov registry record · NA
Study of Soft Contact Lens Use With 7 Day Extended Wear
A NA study, sponsored by CooperVision.
- Completed
- Registry status
- NA
- Development phase
- 460
- Enrollment target
NCT00597467 is a NA study that has completed, run by CooperVision. The registered enrollment target is 460 participants.
The verdict
NCT00597467, a NA study, has completed, sponsored by CooperVision.
- COMPLETED
- Registry status
- NA
- Development phase
- 460 participants
- Enrollment target
Study Summary
To compare the safety and efficacy of the CVI silicone-hydrogel lens worn on an extended wear basis for a period of up to 7 days and 6 nights with the Acuvue 2 soft contact lenses.
Interventions
- DEVICE VISA (comfilcon A) Silicone Hydrogel Soft contact lens
- DEVICE Acuvue 2 Soft Contact Lens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 460 participants |
| Start Date | 2006-03 |
| Est. Completion | 2007-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00597467
The ClinicalTrials.gov registry entry for NCT00597467 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 460 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CooperVision, which has 64 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which VISA (comfilcon A) Silicone Hydrogel Soft contact lens is the first listed.
NCT00597467 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00597467 about?
NCT00597467 is a clinical study titled "Study of Soft Contact Lens Use With 7 Day Extended Wear". To compare the safety and efficacy of the CVI silicone-hydrogel lens worn on an extended wear basis for a period of up to 7 days and 6 nights with the Acuvue 2 soft contact lenses.
What is the current status of trial NCT00597467?
This trial is currently completed. It is a NA study. The enrollment target is 460 participants. The study started on 2006-03. Estimated completion is 2007-11.
What interventions are being tested in trial NCT00597467?
The interventions under investigation include: VISA (comfilcon A) Silicone Hydrogel Soft contact lens (DEVICE), Acuvue 2 Soft Contact Lens (DEVICE).
Who is sponsoring clinical trial NCT00597467?
This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.
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