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NCT01966770 · ClinicalTrials.gov registry record · NA
Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses
A NA study, sponsored by CooperVision.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT01966770 is a NA study that has completed, run by CooperVision. The registered enrollment target is 20 participants.
The verdict
NCT01966770, a NA study, has completed, sponsored by CooperVision.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
The aim of this fitting study is to evaluate the clinical performance of different hydrogel and silicone hydrogel contact lenses.
Interventions
- DEVICE Pair 1 (ocufilcon D / ocufilcon D)
- DEVICE Pair 2 (ocufilcon D / enfilcon A)
- DEVICE Pair 3 (ocufilcon D / comfilcon A)
- DEVICE Pair 4 (methafilcon A / methafilcon A)
- DEVICE Pair 5 (methafilcon A / comfilcon A)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2013-10 |
| Est. Completion | 2013-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01966770
The ClinicalTrials.gov registry entry for NCT01966770 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 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 5 interventions - of which Pair 1 (ocufilcon D / ocufilcon D) is the first listed.
NCT01966770 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01966770 about?
NCT01966770 is a clinical study titled "Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses". The aim of this fitting study is to evaluate the clinical performance of different hydrogel and silicone hydrogel contact lenses.
What is the current status of trial NCT01966770?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2013-10. Estimated completion is 2013-11.
What interventions are being tested in trial NCT01966770?
The interventions under investigation include: Pair 1 (ocufilcon D / ocufilcon D) (DEVICE), Pair 2 (ocufilcon D / enfilcon A) (DEVICE), Pair 3 (ocufilcon D / comfilcon A) (DEVICE), Pair 4 (methafilcon A / methafilcon A) (DEVICE), Pair 5 (methafilcon A / comfilcon A) (DEVICE).
Who is sponsoring clinical trial NCT01966770?
This trial is sponsored by CooperVision, which has 64 total clinical trials registered on ClinicalTrials.gov.
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