Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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12 December 2020 |
Main ID: |
NCT02968290 |
Date of registration:
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14/11/2016 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Quantification of Posterior Capsule Opacification in Pediatric Cataract
Cataract |
Scientific title:
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Quantification of Posterior Capsule Opacity With Software Analysis Comparing Intraocular Lenses Hydrophilic x Hydrophobic in Pediatric Cataracts |
Date of first enrolment:
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May 1, 2016 |
Target sample size:
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30 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02968290 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- indication for cataract surgery
Exclusion Criteria:
- traumatic cataract
- neurological diseases that do not allow the exams
Age minimum:
5 Years
Age maximum:
12 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Posterior Capsule Opacification
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Intervention(s)
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Procedure: Cataract Surgery
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Device: Bausch Lomb AkreosA
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Device: Alcon AcrySof SA60AT
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Primary Outcome(s)
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Opacification of posterior capsule measured by graduation through the software EPCO software
[Time Frame: 360 days after cataract surgery]
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Secondary ID(s)
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University od São Paulo
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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