Laser Cataract Surgery With the Femtosecond Laser Technology
Completed · Phase 4
Conditions studied: Cataracts
In brief
The purpose of this study is to prove the efficacy and safety of the Femtosecond laser to create a clear corneal incision during cataract surgery.
Key facts
- Study ID
- NCT01382823
- Run by
- Innovative Medical
- People needed
- 10
- Starts
- 2010-09-01
- Expected to finish
- 2011-09-01
- Last updated by the study team
- 2011-10-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Study participants must have a cataract for which phacoemulsification extraction and posterior IOL implantation has been planned in at least one eye.
- Study participants should be capable of achieving better than 20/30 Snellen best corrected distance vision after cataract extraction and IOL implantation.
- The surgeon may use the Mento Potential Acuity Meter (PAM)laser interferometer, McIntyre Pinhole, or his/her judgement to estimate the patient's potential acuity.
You may not qualify if…
- Concurrent participation or participation in the last 30 days in other clinical trials.
- Known steroid IOP responder.
- Taking medications that may affect vision, IOP, or ease of cataract surgery (e.g. Flomax, Glaucoma medications, etc.).
- Acute or chronic disease or illness that would increase risk or confound study results(e.g. uncontrolled diabetes mellitus, immunocompromised, etc.).
- Uncontrolled systemic or ocular disease.
- Corneal abnormalities (e.g. stromal, epithelial, or endothelial dystrophies)
- Pseudoexfoliation.
- Ocular hypertension (>or =20hg) or glaucomatous changes in the optic nerve.
Where it is running
- Loden Vision Centers — Goodlettsville, Tennessee, United States
Full record on ClinicalTrials.gov
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