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NCT05776095

Evaluation of Safety and Performance Outcomes of Eyedeal IOL Implantation After Cataract Removal

Status unknown NA Last updated 2 February 2024
What this trial tests

NA trial testing Cataract surgery in Lens Implantation, Intraocular in 97 participants. Status unknown.

Timeline
10 November 2023
Primary endpoint
28 February 2025
28 February 2025

Quick facts

Lead sponsorXi'an Eyedeal Medical Technology Co., Ltd
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment97
Start date10 November 2023
Primary completion28 February 2025
Estimated completion28 February 2025
Sites2 locations across Lithuania, Germany

Drugs / interventions tested

Conditions studied

Sponsor

Xi'an Eyedeal Medical Technology Co., Ltd

Who can join

22 and older, any sex, with Lens Implantation, Intraocular. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A cataract is the clouding of the natural lens in the eye and is very common as when getting older. A cloudy lens makes it difficult to see. A cataract is treated by removing the cloudy lens and replacing it with an intraocular lens (known as an IOL). The goal of this clinical trial is to determine if the Eyedeal® IOL can be safely implanted in a subject's eye and if it can replace efficiently the natural lens. Subjects will be asked to attend a total of seven visits for this study for a period of 12 months after surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Cataract surgery

Trials testing the same drug.

Other recruiting trials for Lens Implantation, Intraocular

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05776095.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing