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Extended Depth of Focus Lenses for Presbyopia
Study Summary
This trial is testing a new contact lens that provides clear distance, intermediate, and near vision. The goal is to quantify the benefits of this new lens design.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- My vision is 20/25 or better with correction.
- Group 1: Presbyopia
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are there any remaining vacancies in this research initiative?
"Affirmative. According to the information posted on clinicaltrials.gov, this medical trial was initial published on September 6th 2022 and is still actively looking for participants as of October 3rd 2022. The study requires a total of 50 patients from one centre."
What is the current enrollment figure for this investigation?
"Correct. Clinicaltrials.gov data shows that this research endeavor, originally posted on September 6th 2022 is presently recruiting individuals to participate in the trial. At present, 50 patients are needed from a solitary clinical site."
Are applicants aged 35 and up eligible to participate in this trial?
"This research study is looking for participants aged 45 to 70."
What potential risks might be associated with NaturalVue Multifocal?
"The safety profile of NaturalVue Multifocal was assigned a score of 3 due to the Phase 4 status, indicating it is approved for use."
Who meets the qualifications to be a participant in this experiment?
"The aim of this research is to recruit 50 individuals aged between 45 and 70 who suffer from presbyopia. It should also be noted that potential participants must have normal corrected vision, the capacity to wear contact lenses, and a need for reading glasses with strength greater than +2.00 diopters."
Who else is applying?
What state do they live in?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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