Phase
Condition
Eye Disorders/infections
Eye Disease
Vision Loss
Treatment
N/AClinical Study ID
Ages 21-99 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Referred for cataract surgery at Parkland Memorial Hospital
Potential post-operative visual acuity of 20/30 or greater determined by potentialacuity meter (PAM) testing or modified super pinhole potential acuity of 20/30 orgreater
Clear intraocular media other than cataract in study eye(s)
Subject eyes will have a dilated pupil diameter of at least 6 mm
Subject eyes will lack other pre‐existing ocular pathology or condition that mayconfound treatment effects, including diabetic retinopathy, previous retinaldetachment, iris neovascularization, amblyopia, optic nerve atrophy or recurrentsevere anterior or posterior segment inflammation of unknown etiology.
Exclusion
Exclusion Criteria:
Severe corneal diseases or prior corneal surgery
Active, significant external ocular or eyelid disease
History of lens abnormalities including posterior polar cataract and zonular weaknessprecluding standard non‐complex cataract surgery
Retinal or posterior segment disease
Advanced glaucoma, white or advanced cataract (precluding adequate examination of theposterior pole)
Anatomic conditions that prevent placement of the femtosecond laser docking ring
Corneal opacity that will interfere with the laser beam (hazy cornea)
Presence of blood or materials in the anterior chamber
Hypotony, advanced glaucoma, or presence of cornea implant
Poor dilating pupil such that the iris is not peripheral to the intended diameter forthe capsulotomy
Condition which would cause inadequate clearance between the intended capsulotomydepth and the corneal endothelium
Any contraindication to cataract or kerato‐refractive surgery
Contact lens wearers must discontinue the use of contacts for an appropriate period oftime to ensure that their corneas are stable before screening measurements areperformed. For rigid gas permeable (RGP) lenses, it is at least 2‐4 weeks beforeaccurate imaging measurements can be performed. Study doctor will assess patientfindings and determine how long RGP lens wear must be discontinued prior to surgery.For soft contact lenses, it is at least 3 days prior to study measurements.
Study Design
Study Description
Connect with a study center
Parkland Memorial Hospital
Dallas, Texas 75235
United StatesSite Not Available
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