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Effect of improved intraocular lenses on contrast sensitivity tests.

Recruiting
Conditions
Each patient will receive a spherical IOL in one eye and an aspherical IOL in the fellow eye. The spherical IOL is normally used, the aspherical is not. The IOL's are CE approved.
Registration Number
NL-OMON23838
Lead Sponsor
niversity Hospital Groningen, department ophtalmologyHanzeplein 1Postbus 30.0019700 RB GroningenThe Netherlands Tel: (+31)050-3612510Fax: (+31)050-3611709AMO (advanced medical optics) Groningen B.V.Van Swietenlaan 59728 NX GroningenTel: (+31)050-5296600 Fax: (+31)050-5267860
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Cataract in both eyes.

Exclusion Criteria

1. Other ocular pathology as diabetic, macula degeneration and glaucoma;
2. Cylinder larger than 1,5 D;
3. Medication that influences the tear function of the eye;
4. Pathology that influences the tear production;
5. Prevalance of pathology between the two cataract operations;
6. Younger than 18 years;
7. Prevalance of senile dementia (MMSE<22).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of the contrast sensitivity in the aspheric IOL.
Secondary Outcome Measures
NameTimeMethod
1. No decrease of depth of focus.<br>2. No difference in intraocular stray light.
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