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Cataract clinical trials

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NCT ID: NCT04161963 Recruiting - Cataract Clinical Trials

Incidence of Sub-clinical Cystoid Macular Edema After Cataract Surgery

ICCME
Start date: March 4, 2019
Phase:
Study type: Observational

Cystoid macular edema (CME) can limit visual acuity after cataract surgery. Little is known whether the incidence is similar between standard ultrasound phacoemulsification cataract surgery (phaco), femtolaser assisted cataract surgery (FLACS), and combined phacoemulsification cataract surgery plus micro invasive glaucoma surgery (phaco+MIGS) procedures.

NCT ID: NCT04138771 Recruiting - Cataract Clinical Trials

Validation of an Artificial Intelligence System for Postoperative Management of Cataract Patients

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

Cataract surgery is the current standard of management for cataract patients, which is typically succeeded by a postoperative follow-up schedule. Here, the investigators established and validated an artificial intelligence system to achieve automatic management of postoperative patients based on analyses of visual acuity, intraocular pressure and slit-lamp images. The management strategy can also change according to postoperative time.

NCT ID: NCT04131114 Recruiting - Glaucoma Clinical Trials

Glaucoma After Congenital And Infantile Cataract Surgery

Start date: January 1, 2011
Phase:
Study type: Observational

Pediatric patients who have undergone surgery for congenital or infantile cataracts have a risk of developing suspected glaucoma and glaucoma, but the current evidence does not address our understanding of the incidence and associated risk factors of suspected glaucoma/glaucoma for application in clinical standard care. Therefore, this study investigated the incidence of and risk factors for suspected glaucoma/glaucoma in patients who have undergone surgery for congenital/infantile cataracts.

NCT ID: NCT04120389 Recruiting - Cataract Clinical Trials

Efficacy of an Ocular Bandage Contact Lens for the Treatment of Dry Eye After Complicated and Combined Cataract Surgery

Start date: March 13, 2020
Phase: N/A
Study type: Interventional

To study the efficacy of an ocular bandage contact lens for the treatment of dry eye after complicated and combined cataract surgery

NCT ID: NCT04082273 Recruiting - Cataract Clinical Trials

Comparison of Femto-laser and Manually Created Clear Corneal Incisions During Cataract Surgery

Z8_CCI
Start date: August 26, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to test the hypothesis, that in terms of Surgically Induced corneal Astigmatism (SIA), Higher-order Aberrations (HOA), and wound geometry the femtosecond clear corneal incisions (CCIs) created during cataract surgery are not inferior when compared to manual CCIs. The potential risks associated with application of the femtosecond laser in this study are no greater or in most cases less than those associated with the standard manual cataract surgical procedure, and the potential benefits (such as precision and reproducibility) are greater than with the standard manual cataract surgery. Therefore, the risk-to-benefit ratio is very low, such that the potential benefits for a subject participating in this study exceed the potential risks

NCT ID: NCT04063358 Recruiting - Cataract Clinical Trials

Anti-VEGF Intravitreous Injections for Diabetic Macular Edema in Patients Undergoing Cataract Surgery

Anti-VEGF
Start date: August 22, 2019
Phase: Phase 3
Study type: Interventional

The investigators aim to evaluate how different timing of anti-VEGF intravitreous injections affect visual acuity (BCVA) in patients with diabetic macular edema who are undergoing cataract surgery; and to evaluate how different timing of anti-VEGF intravitreous affect OCT CSF thickness and total number of postoperative injections in patients with diabetic macular edema who are undergoing cataract surgery.

NCT ID: NCT04050644 Recruiting - Clinical trials for Age-related Cataract

Comparison of Treatment With Preservative-free Dexamethasone 0.1% (Monofree Dexamethason) and Diclofenac 0.1% (Dicloabak) Eye Drops Versus Preserved Dexamethasone 0.1% (Maxidex) and Diclofenac 0.1% (Voltaren Ophtha) Eye Drops After Cataract Surgery

GIST
Start date: October 30, 2018
Phase: Phase 4
Study type: Interventional

To compare treatment with preservative-free dexamethasone 0.1% (Monofree Dexamethason) and diclofenac 0.1% (Dicloabak) eye drops versus preserved dexamethasone 0.1% (Maxidex) and diclofenac 0.1% (Voltaren Ophtha) eye drops after cataract surgery in terms of postoperative inflammation, iatrogenic dry eye disease and cystoid macular edema.

NCT ID: NCT03944070 Recruiting - Clinical trials for Wet Macular Degeneration

Management of Patients With Neovascular Age-related Macular Degeneration Undergoing Cataract Surgery

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

To-date there have been only very few studies to examine the effect of cataract surgery to patients with wet age-related macular degeneration. The evidence on the effects of cataract surgery in such patients suggests improvement of their visual function and quality of life, but at the same time a subclinical susceptibility to macular edema and exacerbation of the choroidal neovascularization. Therefore it is highly important to identify the optimum treatment regime, pursuing the best anatomical and functional postoperative results.

NCT ID: NCT03921762 Recruiting - Cataract Clinical Trials

Comparison of a New EDOF-IOL With a Standard-EDOF-IOL

Start date: October 29, 2018
Phase: N/A
Study type: Interventional

Comparison of the new extended depth of focus (EDOF) intraocular lens (IOL) ARTIS ACTIVE, which is designed as a twinset of IOLs, with the standard EDOF IOL AT Lara .

NCT ID: NCT03908359 Recruiting - Congenital Cataract Clinical Trials

Comparison of the Effect of Minimal Invasive Lens Surgery and Traditional Cataract Surgery

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Previously, the investigators have developed a minimal invasive lens surgery in the purpose of reduce post-operative complications of congenital cataract. This prospective, randomized controlled study aims at comparing the prognosis of the minimal invasive lens surgery and the traditional cataract surgery for treating congenital cataracts.