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NCT05438615 · ClinicalTrials.gov registry record · NA
Corneal Refractive Therapy Design Comparison for -4 to -6 Diopter Treatment for Overnight Wear for Myopia
A NA study, sponsored by CooperVision International Limited (CVIL).
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT05438615 is a NA study that has completed, run by CooperVision International Limited (CVIL). The registered enrollment target is 40 participants.
The verdict
NCT05438615, a NA study, has completed, sponsored by CooperVision International Limited (CVIL).
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
The primary objective of this study is to compare the effectiveness of two proximity control geometry lens designs to treat eyes with pretreatment myopia between -4.00 and -6.00 D myopia with and without refractive astigmatism in a modality involving overnight wearing.
Interventions
- OTHER Corneal Refractive Therapy-spherical
- OTHER Corneal Refractive Therapy-aspherical
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2015-12 |
| Est. Completion | 2016-10-27 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05438615
The ClinicalTrials.gov registry entry for NCT05438615 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CooperVision International Limited (CVIL), which has 11 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Corneal Refractive Therapy-spherical is the first listed.
NCT05438615 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05438615 about?
NCT05438615 is a clinical study titled "Corneal Refractive Therapy Design Comparison for -4 to -6 Diopter Treatment for Overnight Wear for Myopia". The primary objective of this study is to compare the effectiveness of two proximity control geometry lens designs to treat eyes with pretreatment myopia between -4.00 and -6.00 D myopia with and without refractive astigmatism in a modality involving overnight wearing.
What is the current status of trial NCT05438615?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2015-12. Estimated completion is 2016-10-27.
What interventions are being tested in trial NCT05438615?
The interventions under investigation include: Corneal Refractive Therapy-spherical (OTHER), Corneal Refractive Therapy-aspherical (OTHER).
Who is sponsoring clinical trial NCT05438615?
This trial is sponsored by CooperVision International Limited (CVIL), which has 11 total clinical trials registered on ClinicalTrials.gov.
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