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Clinical Trial Summary

The primary objective of LUTEGA is it to determine the long term effect (about 1 year) of the supplementation with a fixed combination of lutein/zeaxanthin and omega-3- fatty acids on the optical density (OD) of macular pigment in patients with non- exudative age related maculopathy.

Furthermore, it is to be examined whether changes of the optical density are different dosages dependent. Possible changes of lipofuscin content and effect on drusen in AMD patients are studied. The measurement of optical density of macular pigment uses the 1- wavelength reflection method recording reflection images at 460 nm by a fundus camera. The patients are investigated at baseline and are followed up over one year in four more visits. In addition to the OD- measurement each examination includes standardized visual acuity test (ETDRS), amsler- grid, slit lamp biomicroscopy, fundus photography (color and autofluorescence) and a blood sample.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00763659
Study type Interventional
Source University of Jena
Contact
Status Completed
Phase N/A
Start date May 2008
Completion date September 2011

See also
  Status Clinical Trial Phase
Completed NCT00494325 - The Role of Macular Pigment in Patients With Age-related Macular Degeneration
Completed NCT01648660 - Long Term Effects of Lutein/Zeaxanthin and Omega-3- Supplementation for Two More Years (LUTEGA 2) N/A
Completed NCT00746668 - A Multi-Center Study of Reading Rehabilitation in Macular Disease N/A
Completed NCT00125632 - Measuring Reading Rehabilitation Outcomes N/A