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NCT01777984 Clinical Trial

Impact of Visceral Fat on the Pathogenesis of Age-related Macular Degeneration

Age-related Macular Degeneration Clinical Trial

Official title:
Impact of Visceral Fat on the Pathogenesis of Age-related Macular Degeneration

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT01777984
Other study ID # EK-08-122-0708
Secondary ID
Status Active, not recruiting
Phase N/A
First received December 1, 2011
Last updated January 24, 2013
Start date December 2009
Est. completion date December 2013

Study information
Verified date January 2013
Source Rudolf Foundation Clinic
Contact n/a
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the relationship among the body fat distribution, especially the visceral fat, in patients with age-related macular degeneration in comparison to patients with a normal fundus.

Description:

In this study the investigators want to examine the relationship among visceral fat, serum leptin levels, and high-sensitive CRP (hsCRP), Tnf-alpha, Amyloid alpha and Amyloid Beta serum levels in patients with age-related macular degeneration in comparison to patients with a normal fundus.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 100
Est. completion date December 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- man and women over 18 years old

- filled informed consent

- diagnosis of age-related macular degeneration

Exclusion Criteria:

- inherited retinal disease

- other acquired retinal macular disease

- missing informed consent

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Austria Rudolf Foundation Clinic Vienna

Sponsors (1)
Lead Sponsor Collaborator
Rudolf Foundation Clinic

Country where clinical trial is conducted

Austria, 

Outcome
Type Measure Description Time frame Safety issue
Primary visceral fat ratio 1 day No
Secondary Leptin, Amyloid, TNF alpha, CRP 1 day No
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