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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01998698
Other study ID # 192/19-11-2013
Secondary ID
Status Completed
Phase N/A
First received November 19, 2013
Last updated January 14, 2017
Start date March 2013
Est. completion date September 2013

Study information

Verified date January 2017
Source Democritus University of Thrace
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators would like to assess whether monovision correction of multifocal lens insertion provides more satisfaction to cataract patients following an uncomplicated phacoemulsification surgery.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender All
Age group 60 Years to 75 Years
Eligibility Inclusion Criteria:

- Bilateral senile cataract

Exclusion Criteria:

- Glaucoma

- Corneal pathology

- Fundus pathology

- Severe neurological/mental diseases that interfere with visual acuity

- Former intraocular operation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Phacoemulsification surgery
Phacoemulsification surgery with intraocular lens implantation and monovision correction
Phacoemulsification surgery
Phacoemulsification surgery with multifocal intraocular lens implantation

Locations

Country Name City State
Greece University Hospital of Alexandroupolis Alexandroupolis Evros

Sponsors (1)

Lead Sponsor Collaborator
Democritus University of Thrace

Country where clinical trial is conducted

Greece, 

References & Publications (1)

Labiris G, Giarmoukakis A, Patsiamanidi M, Papadopoulos Z, Kozobolis VP. Mini-monovision versus multifocal intraocular lens implantation. J Cataract Refract Surg. 2015 Jan;41(1):53-7. doi: 10.1016/j.jcrs.2014.06.015. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary VF14 score 6 months following operation
Secondary Distant Visual Acuity 6 months following surgery
Secondary Near Vision visual acuity 6 months following surgery
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