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NCT06220331Completed

Data Collection After Intensity IOL Implantations

Intensity Lenses Post Operation Standard of Care Visits - Data Collection.
Hanita LensesClinicalTrials.govdeviceDevice trial
Verified
Study focus
Disease/Condition
Cataract
Drug/Device/Intervention
Intra Ocular Lens
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
Hanita Lenses
Location
Buenos Aires, Argentina
Timeline & enrollment
Phase
N/A
Start date
Jul 13, 2023
End date
Sep 30, 2023
Enrollment
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 cataractCataract, unspecifiedComplicated cataractOther specified cataractSenile cataract
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06220331
Type
Device Trial
About this record

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.