Sakarya University Ophthalmology Department
Sakarya, Turkey (Türkiye)
NCT Number: NCT04140383
This study evaluates and compares clinical outcomes of < 85 and ≥ 85 year old patients who underwent cataract surgeries.
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Notify Me65 year–95 year
All sexes
Observational
Sakarya, Turkey (Türkiye)
The medical records of patients who were underwent cataract surgery between January 2014 and October 2017 were investigated retrospectively and patients 65 years and older were recruited. Two groups were made according to age: group1 composed of patients age range between 65 and 85 years and group 2 composed of patients 85 years and older. Gender, presence of diabetes mellitus (DM), hypertension (HT), drug use were noted.
The results of best corrected visual acuity (BCVA) converted to LogMar, intraocular pressure (IOP) before and 3 months after operation, biomicroscopic and fundus examinations were investigated.
Additional ocular diseases such as glaucoma, age related macular degeneration (AMD), pseudoexfoliation syndrome, retinopathies and maculopathies related to systemic diseases were noted. Pupil dilation properties were also noted as poor, mid or full pupil dilation.
Cataract surgery techniques such as phacoemulsification, extra- and intracapsular lens extractions, peroperative complications, intracameral drug use were investigated.
these aforementioned outcomes evaluated and compared between groups.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Cataract surgery was performed by using phacoemulsification technique, routinely. But other techniques for instance extra or intracapsular cataract extraction (ECCE, ICCE) techniques were performed when needed. Phacoemulsification technique was performed by 2 experienced surgeon (G.A. and E.C.) under topical anesthesia, thorough limbal incision. Foldable single piece hydrophobic acrylic intraocular lens (IOL) was inserted in the bag. In the presence of complications related to anterior or posterior capsules, 3 pieces IOL was preferred. When ECCE technique was chosen, single piece polymethyl methacrylate IOL was inserted.
Time frame: Before cataract surgery
Best corrected visual acuity converted to LogMar
Time frame: three months after cataract surgery
Best corrected visual acuity converted to LogMar
Time frame: Baseline (Before cataract surgery)
number of participants who have diabetes mellitus
Time frame: before cataract surgery
number of participants who have essential hypertension
Time frame: before cataract surgery
number of participants who have a history of acetylsalicylic acid use
Time frame: before cataract surgery
number of participants who have a history of oral flomax use
Time frame: Baseline (Before cataract surgery)
number of participants who have age related macular degeneration
Time frame: before cataract surgery
number of participants who have glaucoma
Time frame: before cataract surgery
number of participants who have pseudoexfoliation
Time frame: During cataract surgery
number of participants who have poor pupil dilation
Time frame: During cataract surgery
number of participants who have zonule deficiency
Time frame: Baseline (Before cataract surgery)
number of participants who have nuclear, posterior subcapsular, corticonuclear, mature, nigra, traumatic cataract
Time frame: During cataract surgery
measurement of effective phacoemulsification time in participants who underwent cataract surgery
Time frame: During cataract surgery
participants who had posterior capsule rupture during surgery
Time frame: during surgery
number of participants who needed anterior vitrectomy during cataract surgery
Time frame: 3 months after cataract surgery
number of participants who left aphakic after cataract surgery
Time frame: during surgery
number of participants who needed intracameral adrenalin use
Sakarya University
Other
Outcomes of Cataract Surgeries in Patients With Advanced Age
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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