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NCT02024698 · ClinicalTrials.gov registry record · NA
Multi-center Clinical Evaluation of PC 1-Day vs 1-Day Acuvue Moist
A NA study, sponsored by CooperVision.
- Completed
- Registry status
- NA
- Development phase
- 43
- Enrollment target
NCT02024698: Completed NA study, sponsored by CooperVision.
NCT02024698 is a NA study that has completed, run by CooperVision. The registered enrollment target is 43 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02024698, a NA study, has completed, sponsored by CooperVision.
- COMPLETED
- Registry status
- NA
- Development phase
- 43 participants
- Enrollment target
Study Summary
The objective of this study is to compare the clinical performance of ProClear 1-Day versus 1-Day Acuvue Moist each for one week of daily disposable wear.
Primary Outcome
Subjective Assessment of comfort on insertion at baseline for each pair using questionnaire and rated on subjective response scale. (0-10; 0= very uncomfortable, 10=cannot feel)
Interventions
- DEVICE etafilcon A
- DEVICE omafilcon A
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 43 participants |
| Start Date | 2014-01 |
| Est. Completion | 2014-03 |
| Phase | NA |
What the finished NCT02024698 record still lists
NCT02024698 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which etafilcon A is the first listed.
NCT02024698 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02024698 about?
NCT02024698 is a clinical study titled "Multi-center Clinical Evaluation of PC 1-Day vs 1-Day Acuvue Moist". The objective of this study is to compare the clinical performance of ProClear 1-Day versus 1-Day Acuvue Moist each for one week of daily disposable wear.
What is the current status of trial NCT02024698?
This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2014-01. Estimated completion is 2014-03.
What interventions are being tested in trial NCT02024698?
The interventions under investigation include: etafilcon A (DEVICE), omafilcon A (DEVICE).
Who is sponsoring clinical trial NCT02024698?
This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02024698's enrollment target sits among peer trials
43 1435th of 2000 higher than 565 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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