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Data Collection After Intensity IOL Implantations - Trial NCT06220331

Access comprehensive clinical trial information for NCT06220331 through Pure Global AI's free database. This phase not specified trial is sponsored by Hanita Lenses and is currently Completed. The study focuses on Cataract. Target enrollment is 31 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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NCT06220331
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Trial Details
ClinicalTrials.gov โ€ข NCT06220331
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Data Collection After Intensity IOL Implantations
Intensity Lenses Post Operation Standard of Care Visits - Data Collection.

Study Focus

Cataract

Intra Ocular Lens

Observational

device

Sponsor & Location

Hanita Lenses

Buenos Aires, Argentina

Timeline & Enrollment

N/A

Jul 13, 2023

Sep 30, 2023

31 participants

Primary Outcome

The aim of this study is to evaluate performance of Hanita Lenses Intensity SL IOL.

Summary

Hanita Lenses new Intensity IOL and Intensity Toric were been designed to have very high
 efficiency of light leading to a high MTF, wide focal ranges of far, intermediate and near
 vision and minimal loss of light energy. The main purpose of this study is to collect
 existing post-operative data based on standard of care follow up visits at the clinic.

ICD-10 Classifications

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

Data Source

ClinicalTrials.gov

NCT06220331

Device Trial