ReLux-AMD: Rheohemapheresis and Lutein Supplementation in the Non-Exsudative Form of Age-Related Macular Degeneration

Sponsor
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery (Other)
Overall Status
Unknown status
CT.gov ID
NCT00443911
Collaborator
(none)
20
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62
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Study Details

Study Description

Brief Summary

Age-related macular degeneration is one of the major causes of blindness in the western world. There is an exsudative and a non-exsudative form of age-related macular degeneration.Most studies concentrate on the exsudative form. In the non-exsudative form the policy is generally watch and see, but patients are at risk to develop an exsudative form. So far, the only accepted therapy to reach stable disease in the non-exsudative form is high-dose supplementation of antioxidants. Another approach to improve visual acuity in patients with non-exsudative form of macular degeneration is rheohemapheresis treatment, an extracorporeal therapy where plasma is separated from blood cells. By the use of a hollow fiber filter plasma is depleted of high molecular weight proteins and reinfused. Others report describe the supplementation of lutein (a vitamin A derivative) as possible treatment option. However, none of the studies have yet examined a combination of rheohemapheresis and lutein supplementation.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Rheohemapheresis will be performed in 5 cycles. One cycle consists of 2 rheohemapheresis treatments on day 1 and day 4. A cycle lasts for 4 weeks and will be repeated every fourth week. During each treatment > 75% to 100% of patients total plasma volume has to be filtered.General medical reviews, ETDRS and Radner visual acuity assessment, ophthalmologic examinations, ocular imaging with OCT 3, autofluorescein imaging and infrared imaging, multifocal ERG, ocular echography, and blood examinations will be performed.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    20 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Rheohemapheresis and Lutein Supplementation (Xantophyll Carotenoid) in the Non-Exsudative Form of Age-Related Macular Degeneration
    Study Start Date :
    Mar 1, 2007
    Anticipated Study Completion Date :
    May 1, 2012

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      50 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Study eye with non-exsudative AMD AREDS II - III

      • with > 10 large soft, and / or confluent drusen within 3000 nm of the foveal centre

      • and a best corrected visual acuity of 0.06 - 1.0 using ETDRS charts (letter score of 3 to 50 letters)

      • with / without geographic atrophy less than 3 disc diameters within 3000 nm of the foveal centre ยด. with / without serous pigment epithelial detachment without clearly identifiable neovascularisation

      • Patients must have elevated baseline concentrations of at least one of the rheologic parameters (serum cholesterol level > 200 mg/dL, fibrinogen level > 390 mg/dL, or plasmaviscosity > 1.6 mPa*s)

      • Men or women aged between 50 - 99 years.

      Exclusion Criteria:
      • Study eye with exsudative AMD

      • Study eye with concomitant retinal or choroidal disorder other than AMD

      • Study eye with significant central lens opacities and / or conditions that limit the view of the fundus

      • poor general condition

      • hematocrit < 30%

      • coagulation disorders (incl. marcoumar therapy)

      • significant cardiac problems ( > NYHA II)

      • history (< 12 months) of cardiac infarction

      • uncontrolled arterial hypertension

      • recent history (< 3 months) of cerebral vascular infarction

      • cerebrovascular disease IV

      • uncontrolled diabetes

      • insufficient antecubital venous access

      • lutein supplementation within the last 3 months

      • weight < 45 kg

      • hemato-oncological disorder

      • Patients who are unwilling to adhere to visit examination schedules

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Rudolf Foundation Clinic, Department of Ophthalmology Vienna Austria 1030

      Sponsors and Collaborators

      • The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery

      Investigators

      • Principal Investigator: Katharina E Kubista, MD, LBI

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00443911
      Other Study ID Numbers:
      • LBI-06-053-0406
      First Posted:
      Mar 7, 2007
      Last Update Posted:
      Jun 27, 2011
      Last Verified:
      Jun 1, 2011
      Keywords provided by , ,
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Jun 27, 2011