Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-26 @ 2:39 PM
Ignite Modification Date:
2025-12-26 @ 2:39 PM
NCT ID:
NCT05250206
Brief Summary:
Evaluation of the efficacy in decreasing myopia progression of the proposed ophthalmic lens prototypes.
Detailed Description:
A prospective, double-blind, randomized clinical trial (RCT) to analyze the effect of a new ophthalmic lens prototype on myopia progression. The follow-up period to evaluate the efficacy of the lens will be 3 years including a total of 5 visits.
The sample will consist of a group of 92 myopic children who will be randomly assigned to one of the treatment groups:
* Control group who will receive standard monofocal lenses.
* Treatment group who will wear a prototype lens based on peripheral positive defocus.
Study:
NCT05250206
Study Brief:
Protocol Section:
NCT05250206