Satisfaction & Spectacle Independence With ReSTOR 2.5 & ReSTOR 3.0 IOLs
Completed
Conditions studied: Cataract
In brief
Patients implanted with the ReSTOR 2.5 multifocal IOL in the dominant eye and the ReSTOR 3.0 in the non-dominant eye have overall satisfaction and spectacle independence at least comparable to that with bilateral implantation of the 3.0 add lens. Glare and haloes and other unwanted visual side effects with this mixed combination of lenses is better than with bilateral 3.0 lenses.
Key facts
- Study ID
- NCT03073681
- Run by
- MDbackline, LLC
- People needed
- 100
- Starts
- 2017-03-03
- Expected to finish
- 2019-05-22
- Last updated by the study team
- 2019-06-05
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients implanted with either a ReSTOR 2.5 or 3.0 multifocal within 24 months of the survey administration.
- Patients with otherwise healthy eyes, not exhibiting any significant ocular morbidity that would be expected to influence outcome measures.
You may not qualify if…
- Patients with visually significant co-morbidities (corneal, retina, optic nerve disease) that could affect their satisfaction with surgery
- Patients with surgical complications either during or after surgery (capsule tears, iris trauma, decentered IOL, cystoid macular edema, etc.)
- Patients with previous refractive surgery
- Patients with ≥ grade 1 posterior capsule opacity at their last visit
Where it is running
- Harvard Eye Associates — Laguna Hills, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.