Prospective Clinical Study of Preoperative and Postoperative Unilateral Mild Cataract Patients (NCT04266847) | Clinical Trial Compass
UnknownNot Applicable
Prospective Clinical Study of Preoperative and Postoperative Unilateral Mild Cataract Patients
China60 participantsStarted 2019-10-30
Plain-language summary
This is to compare preoperative and postoperative binocular functional vision in patients with unilateral intraocular len(IOL) in one eye and mild cataract in the fellow eye.
Who can participate
Age range50 Years – 80 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients who had monocular intraocular lens in one eye with mild cataract in the fellow eye ask for the cataract surgery in the fellow eye
* Regular corneal topography and corneal astigmatism ≤ 0.75 Diopter
Exclusion Criteria:
* Pregnant or nursing women
* In the presence of other ocular diseases that may affect the stability of the lens capsule (pseudoexfoliation syndrome, glaucoma, traumatic cataract, Marfan syndrome, etc.)
* In the presence of other ocular diseases that is expected to have a poor final visual acuity of worse than 0.2 logMAR after surgery (amblyopia, strabismus, keratoconus, etc.)
* Pupil abnormality (non-reactive pupil, tonic pupils, abnormally shaped pupils, etc.)
* Patients using systemic or ocular medication that affect visual acuity.
* Patients with history of ocular trauma or prior ocular surgery including refractive procedures
* Patients participating in other clinical trials during the study.