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Age-related Cataract clinical trials

View clinical trials related to Age-related Cataract.

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NCT ID: NCT06266962 Completed - Cataract Clinical Trials

Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome

Start date: July 1, 2020
Phase: Phase 4
Study type: Interventional

Intraoperative Floppy Iris Syndrome (IFIS) is a potentially serious cataract surgery complication. IFIS is most commonly associated with the chronic use of tamsulosin and other alpha1-adrenergic receptor antagonists prescribed in low urinary tract symptoms. There are a number of guidelines for operative technique modifications with the aim to prevent the development of IFIS. The study focuses on two options for prophylactic strategies: the application of atropine drops and the instillation of intracameral epinephrine.

NCT ID: NCT05573529 Completed - Clinical trials for Age-related Cataract

EDOF and Multifocal IOL Study

Start date: November 9, 2020
Phase: N/A
Study type: Interventional

The investigational devices are approved intraocular lenses (IOLs) intended to be implanted after phacoemulsification in individuals suffering from age-related cataract with the need of cataract surgery. Cataract surgery with precedent bilateral randomized IOL implantation will be performed in subjects who have signed an informed consent form. Postoperative examinations will be implemented in accordance with the approved investigational plan.

NCT ID: NCT05148741 Completed - Clinical trials for Age-related Cataract

Evaluation of Capsular Bag Shape Changes After Plate-haptic Intraocular Lens Implantation by SS-OCT

Start date: July 1, 2020
Phase:
Study type: Observational [Patient Registry]

Evaluation of capsular bag shape changes after plate-haptic intraocular lens implantation by SS-OCT.

NCT ID: NCT04702802 Completed - Clinical trials for Age-related Cataract

Clinical Study to Evaluate the Safety of the Viscoelastic Substance PRO-149 When Used During Phacoemulsification, Compared to Healon® EndoCoat.

PRO-149
Start date: September 7, 2021
Phase: Phase 1
Study type: Interventional

Pilot, controlled, parallel group, open, randomized clinical trial to evaluate the safety of the viscoelastic substance PRO-149 (sodium hyaluronate 3%) after trans-surgical administration as a device in performing phacoemulsification and intraocular lens implantation in 36 patients with age-related cataract, compared to Healon® EndoCoat (sodium hyaluronate 3%).

NCT ID: NCT04262596 Completed - Clinical trials for Age-related Cataract

Effectiveness of an Interactive Consulting System to Enhance Patients' Decision-making: A Randomized Controlled Trial

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

To compare the effectiveness of an interactive mobile chatbot and traditional decision aid booklets to enhance informed decisions made by cataract patients. The chatbot was built based on large language models, and could generate ChatGPT-level responses.

NCT ID: NCT04187157 Completed - Cataract Clinical Trials

Association Between Light Spectrum and Survival After Cataract Surgery

Start date: January 1, 2012
Phase:
Study type: Observational

This study was a retrospective observational cohort analysis of subjects aged 65 years and older, who underwent bilateral cataract surgery within a single (15 hospital) healthcare system, to determine the association between type (conventional or blue-light filtering) of implanted intraocular lens and survival.