Measuring of Neuro-visual Functionality With Ocusweep
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|ClinicalTrials.gov Identifier: NCT02258113|
Recruitment Status : Recruiting
First Posted : October 7, 2014
Last Update Posted : October 17, 2017
|Condition or disease||Intervention/treatment||Phase|
|Visual Impairment||Device: Ocusweep||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||600 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Measuring of Neuro-visual Functionality With New Human Visual System Device Ocusweep|
|Study Start Date :||November 2014|
|Estimated Primary Completion Date :||December 2017|
|Estimated Study Completion Date :||December 31, 2017|
LEA numbers, Pelli-Robson, Octopus
Comparable generally used method for measuring visual acuity, contrast sensitivity and visual field.
A novel reaction-time based visual field device.
- Visual acuity [ Time Frame: One visit per one patient (1h/visit) ]Visual acuity is measured as logMAR unit at the one visit for each patient using a novel reaction-time based visual field device and comparable method.
- Contrast sensitivity [ Time Frame: One visit per one patient (1h/visit) ]Contrast sensitivity is measured as logCS unit at the one visit for each patient using a novel reaction-time based visual field device and comparable method.
- Reaction time [ Time Frame: One visit per one patient (1h/visit) ]Reaction time is measured using a novel reaction-time based visual field device and compared with generally used visual field program.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02258113
|Contact: Marika Ojala, Mrsfirstname.lastname@example.org|
|Contact: Markku Leinonen, Dremail@example.com|
|Turku, Finland, 20100|
|Contact: Marika Ojala, MSc firstname.lastname@example.org|
|Contact: Markku Leinonen, Dr email@example.com|