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Clinical Trial Summary

Population 1:

Measure the effect of size glasses from1-9% on stereopsis

Population 2:

Measure the effect of size glasses from 1-9% on stereopsis in two settings:

- before and after cataract surgery

- after dilation of the eye


Clinical Trial Description

Population 1:

21 eye healthy phakic individuals. Measurements: baseline stereopsis and stereopsis after size glass (1-9%) is added in front of the right eye and in front og the left eye. This measurement provides details on how much size difference a person can endure without impairing stereopsis.

Population 2:

11 phakic eye healthy individuals awaiting cataract operation on both eyes. Measurements are the same as population 1 but this study group is also measured after dilating the eyes. This is to see if accommodation affects the measurement. A postoperative measurement six weeks after cataract operation is also performed to examine if cataract operation affects the measurement. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03832335
Study type Observational
Source Glostrup University Hospital, Copenhagen
Contact
Status Recruiting
Phase
Start date July 2015
Completion date December 2020

See also
  Status Clinical Trial Phase
Recruiting NCT05325021 - Correction of Anisometropic Amblyopia in Children.