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NCT03661593 Clinical Trial

Aniseikonia in Epiretinal Membrane Patients

Epiretinal Membrane Clinical Trial

Official title:
Aniseikonia in Epiretinal Membranes

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03661593
Other study ID # H-16020057
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date November 2019

Study information
Verified date September 2018
Source Glostrup University Hospital, Copenhagen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Examination of aniseikonia in epiretinal membranes patients before and after surgery

Description:

Phakic patients woth epiretinal membranes are examined for aniseikonia and refractive status before and after surgery. Follow up is one year.

Recruitment information / eligibility
Status Recruiting
Enrollment 25
Est. completion date November 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Epiretinal membrane Phakic on both eyes

Exclusion Criteria:

- no previous eye surgeries

- refractive status +/- 2 seq

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Cataract guideline
The patients gets an IOL according to cataract guideline correcting the ametropia

Locations
Country Name City State
Denmark Eye department, Nordre ringvej 56 Copenhagen Glostrup

Sponsors (1)
Lead Sponsor Collaborator
Glostrup University Hospital, Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Aniseikonia Measure amount of aniseikonia by measuring aniseikonia with both computer program aniseikonia inspector and the New Aniseikonia test 1 year
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