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Cataract clinical trials

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NCT ID: NCT04468308 Recruiting - Senile Cataract Clinical Trials

VRQOL in Cataract Patients During the COVID-19 Pandemic

Start date: September 8, 2020
Phase:
Study type: Observational

The aim of this questionnaire survey is to evaluate the improvement in vision-related quality of life before and after cataract surgery using the National Eye Institute Visual Function Questionnaire 25 and the delay of improvement in the COVID-19 pandemic.

NCT ID: NCT04465344 Recruiting - Cataract Clinical Trials

Multicentric Clinical Study on Isatis TF Trifocal Intraocular Lens

Start date: May 31, 2021
Phase: N/A
Study type: Interventional

The study will be a multicentric, prospective open-label ethics committee approved clinical study to investigate safety, visual outcomes, contrast sensitivity and rotational stability after bilateral implantation of Isatis TF IOL following cataract surgery.

NCT ID: NCT04457999 Recruiting - Dry Eye Clinical Trials

Clinical Outcome of Lipiflow Treatment Prior to Cataract Surgery in Dry Eye Patients

Start date: March 20, 2020
Phase: N/A
Study type: Interventional

To investigate the clinical outcome of Lipiflow treatment prior to cataract surgery in patients with meibomian gland dysfunction and dry eye disease

NCT ID: NCT04443101 Recruiting - Clinical trials for Age-related Cataract

Effective Lens Position After Cataract Surgery

Start date: January 1, 2019
Phase:
Study type: Observational

Cataract patients were implanted with different types of intraocular lenses for grouping. SSOCT scanning was used to measure ELP and optometry.

NCT ID: NCT04387721 Recruiting - Astigmatism Clinical Trials

Influence of Residual Astigmatism on Visual Acuity in Patients Undergoing Cataract Surgery With Trifocal Intraocular Lens Implantation

Start date: July 29, 2019
Phase:
Study type: Observational

MAIN OBJECTIVE: To assess the influence of residual astigmatism on visual acuity in the different lens foci in patients operated on for cataracts with a trifocal intraocular lens implant. SECONDARY OBJECTIVE: To study the influence of residual astigmatism on the visual quality of the patient in the far focus and to determine if there are differences of affectation in the two study groups.

NCT ID: NCT04362241 Recruiting - Clinical trials for Retinopathy, Diabetic

DEXTENZA VS. PREDNISOLONE ACETATE 1% Macular Edema With Diabetic Retinopathy After Cataract Surgery

Start date: August 7, 2020
Phase: Phase 4
Study type: Interventional

The complicated schedules for administering topical steroid eye drops combined with forgetfulness and physical difficulties instilling the drops may compromise compliance; which in turn could increase the risk for secondary complications such as PME post-cataract surgery, especially in a high-risk diabetic population. Dextenza, a sustained- release steroid insert, could help preclude adherence difficulties and provide better bioavailability, being as effective as, or more effective than steroid drops in preventing PME. The aim of this study is to assess the incidence of PME in diabetic patients undergoing cataract surgery when comparing the Dextenza insert to topical prednisolone acetate 1% drops.

NCT ID: NCT04357249 Recruiting - Pediatric Cataract Clinical Trials

Outcome of Capsular After Pediatric Cataract Surgery With Primary Intraocular Lens Implantation

Capsular
Start date: March 1, 2015
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to evaluate the outcome of capsular in children with cataract, and to explore potential preoperative structural clues for postoperative glaucoma. The investigators included children with cataract planning to have cataract surgery in our institute. Exclusion criteria were: a history of ocular trauma, a history of intraocular surgery, preoperative glaucoma, steroid use before surgery, a history of maternal rubella syndrome, chronic anterior uveitis, persistent fetal vasculature, ocular anomalies associated with an increased risk of glaucoma, unable to complete examinations. The investigators recorded age at surgery, gender and relevant ocular and systemic histories. All patients underwent slit lamp biomicroscopy, slit lamp adapted anterior segment photography.All patients were examined at 1 week, 1 month, 3 months, 6 months, 1 year, 18 months, and two years after surgery. Patients were followed for two years or until the development of severe VAO requiring Nd: YAG laser capsulotomy, whichever came first. The examinations consisted of visual acuity, IOP measurement by a Tonopen tonometer (Reichert, Inc., Seefeld, Germany), fundoscopy, an assessment by high-resolution digital retroillumination imaging (detailed protocol presented below).The primary outcomes were the areas of the posterior capsular opening at different postoperative follow-up visits and during operation.A paired T test was used to compare the areas of the PCO between the postoperative visits and baseline.

NCT ID: NCT04353843 Recruiting - Cataract Clinical Trials

Identification of Clinical, Biometrical and Operatory Factors Related to Pain During Cataract Surgery

Start date: May 1, 2020
Phase:
Study type: Observational

Adults who undergo cataract surgery will be questioned after surgery about the eventual pain they experienced, about their health history, personal treatment. If they accept to be included in the study we'll record different parameters related to the surgery: type of anesthesia, duration of surgery, machines used, unexpected events, particularities noticed by the surgeon, etc. There will be no unusual intervention, everything will be run exactly as if there was no study. No additional consultation needed.

NCT ID: NCT04340635 Recruiting - Cataract Clinical Trials

Multi-center Ocular Biological Parameters Study

Start date: January 1, 2018
Phase:
Study type: Observational

This study is a multi-center study, which collects data from multiple regions to obtain the general biological characteristics of the Chinese population. The formula for calculating the artificial lens power based on foreign populations is effectively modified based on the Chinese population.

NCT ID: NCT04323982 Recruiting - Congenital Cataract Clinical Trials

Comparison of Traditional Cataract Surgery and Traditional Surgery Combined Triamcinolone Staining

Start date: March 27, 2020
Phase: N/A
Study type: Interventional

Previously, the investigators have developed a surgical technique to reduce inflammatory response after congenital cataract surgery. This prospective, randomized controlled study aims to compare the prognosis of traditional cataract surgery with traditional surgery combined triamcinolone staining of the anterior vitreous in treating congenital cataracts.