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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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11 July 2016 |
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Main ID: |
NCT02767284 |
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Date of registration:
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04/05/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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A Comparative Study of Six Methods to Measure Human Contrast Vision
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Scientific title:
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UCST Studie 1 - Jämförande Studie Mellan några Befintliga Och Nyutvecklade Metoder för Att mäta Den Spektrala kontrastkänslighetsfunktionen Hos människa |
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Date of first enrolment:
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June 2016 |
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Target sample size:
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40 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02767284 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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Sweden
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Contacts
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Name:
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Lars Malmqvist, M.D |
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Address:
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Telephone:
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+46186115135 |
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Email:
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lars.malmqvist@neuro.uu.se |
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Affiliation:
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Name:
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Prof. Per Söderberg, M.D PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Uppsala University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Normal best corrected visual acuity: LogMAR = 0
- No current or previous eye disease in either eye.
- Student at Uppsala University
Exclusion Criteria:
- Previous surgery in any eye
- Inability to follow the test procedure.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Methods to Measure Contrast Vision
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Intervention(s)
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Device: Quick-CSF (QCSF)
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Device: UCST-V3
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Device: UCST-V2
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Device: Optec 6500
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Device: Pelli-Robson
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Device: UCST-V1
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Primary Outcome(s)
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Average area under the curve for the log contrast sensitivity function (AULCSF) in one eye for each method
[Time Frame: At end of data collection (up to 12 months after first subject is included)]
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Average time (in seconds) used to measure the contrast sensitivity function for one eye for each method
[Time Frame: At end of data collection (up to 12 months after first subject is included)]
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Secondary Outcome(s)
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Sources of variability of the average area under the curve for the log contrast sensitivity function [AULCSF squared]
[Time Frame: At end of data collection (up to 12 months after first subject is included)]
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Sources of variability of the average time used to measure the contrast sensitivity function [seconds squared]
[Time Frame: At end of data collection (up to 12 months after first subject is included)]
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Secondary ID(s)
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UCST-01.2014
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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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