Clinical Trial on the Visual Function of Enhanced Monofocal and EDoF Intraocular Lenses

ConditionCataract
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-80
SponsorFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

About this trial

Randomized clinical trial to evaluate the visual performance of enhanced monofocal and extended depth-of-field intraocular lenses

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with bilateral cataracts at different stages of development.

Patients with functional visual demands.

Age between 45 and 80 years.

Male or female sex.

Disqualifiers

Vitreous loss.

Pupillary trauma.

Factors likely to affect the medium-term performance of the intraocular lens: Zonular damage, Capsulorhexis tear or injury, Capsular rupture, Endothelial damage.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intraocular lens

    Device

    Implantation of intraocular lens

Treatment groups

90 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Group A: Group 1: Implantation of the Clareon Vivity intraocular lensExperimental treatment 1 intervention
Group B: Group 2: Implantation of the TECNIS Eyhance intraocular lensExperimental treatment 1 intervention
Group C: Group 3: Implantation of the RayOne EMV intraocular lensExperimental treatment 1 intervention
Group D: Group 4: Implantation of the IsoPure Serenity intraocular lensExperimental treatment 1 intervention
Group E: Group 5: Implantation of the Vivinex Impress intraocular lensExperimental treatment 1 intervention
Group F: Group 6: Implantation of the TECNIS PureSee intraocular lensExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual acuity at different distances

Far vision, intermediate vision, near vision

Time frame
1 month, 3 months, 6 months
2

Dysphotopsias

Dysphotopsias after the IOL implantation

Time frame
1 month, 3 months, 6 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: