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NCT05704686

Clinical Outcomes of an New EDOF IOL (Isopure®)

Completed Last updated 30 January 2023
What this trial tests

trial testing Isopure 1.2.3 intraocular EDOF lens implantation in Lens Opacities in 62 participants. Completed in 31 December 2021.

Timeline
26 April 2021
Primary endpoint
31 December 2021
31 December 2021

Quick facts

Lead sponsorKristof Vandekerckhove, MD, MBA
StatusCompleted
Study typeOBSERVATIONAL
Enrollment62
Start date26 April 2021
Primary completion31 December 2021
Estimated completion31 December 2021
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Kristof Vandekerckhove, MD, MBA

Who can join

50 and older, any sex, with Lens Opacities or Cataract. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Single-center, retrospective, open-label observational study aiming to evaluate visual outcomes and patient satisfaction after bilateral implantation of Isopure® EDOF-IOL with a mono-minovision target.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Lens Opacities

Currently open trials in the same condition.

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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/NCT05704686.

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