Cataract Refractive Suite Study
| Status: | Terminated |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | 22 - Any |
| Updated: | 9/16/2018 |
| Start Date: | March 2, 2017 |
| End Date: | July 25, 2017 |
A Prospective, Multicenter, Randomized Evaluation of Refractive Predictability in Patients With or Without Corneal Astigmatism (Maximum Allowable up to 1.25D) When Using the Cataract Refractive Suite and Standard Manual Techniques
The purpose of this study is to compare the refractive predictability (prediction error)
between the Cataract Refractive Suite (CRS) and standard manual technique at one month
post-operative
between the Cataract Refractive Suite (CRS) and standard manual technique at one month
post-operative
Inclusion Criteria:
- Diagnosed with bilateral cataracts;
- Planned cataract surgery and implantation of ReSTOR +2.5 D multifocal intraocular lens
(IOL) in both eyes;
- Clear intraocular media, other than cataract, in study eye(s);
- Willing and able to complete all required postoperative visits;
- Able to comprehend and sign a statement of informed consent;
- Other protocol-specified inclusion criteria may apply.
Exclusion Criteria:
- Significant irregular corneal astigmatism;
- History of or current severe dry eyes, retinal/uveal pathology or concurrent ocular
disease;
- Previous intraocular or corneal refractive surgery, corneal transplant, or retinal
detachment;
- Any inflammation or edema (swelling) of the cornea;
- Pregnant;
- Other protocol-specified exclusion criteria may apply.
We found this trial at
3
sites
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