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Efficacy of the AkkoLens IOL in Patients With Cataract - Trial NCT06231784

Access comprehensive clinical trial information for NCT06231784 through Pure Global AI's free database. This phase not specified trial is sponsored by Vissum, Instituto Oftalmológico de Alicante and is currently Completed. The study focuses on Cataract. Target enrollment is 25 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06231784
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Trial Details
ClinicalTrials.govNCT06231784
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Efficacy of the AkkoLens IOL in Patients With Cataract
Prospective, Open-label Clinical Study to Evaluate the Efficacy and Function of the AkkoLens Accommodative Intraocular Acrylic Lens for the Treatment of Cataracts

Study Focus

Cataract

LUMINA IOL

Interventional

device

Sponsor & Location

Vissum, Instituto Oftalmológico de Alicante

Timeline & Enrollment

N/A

Jun 09, 2016

Dec 01, 2023

25 participants

Primary Outcome

Distance Vision measurements,Defocus curve measurements,Accommodation measurements,Depth of focus measurements

Summary

The goal of this observational study is to learn about the verification of the effectiveness
 and visual acuity of LUMINA in patients after lens replacement due to cataracts.
 
 The main questions it aims to answer are:
 
 - Evaluation of the effectiveness of the LUMINA lens in patients after lens replacement
 due to cataracts
 
 - Evaluation of the accommodative power of the LUMINA lens. Participants will have
 cataract surgery and the IOL LUMINA will be implanted in the sulcus.

ICD-10 Classifications

Other cataract
Cataract, unspecified
Complicated cataract
Other specified cataract
Senile cataract

Data Source

ClinicalTrials.gov

NCT06231784

Device Trial