May 2003
Volume 44, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2003
Prospective Comparative Study on Intravitreal Triamcinolone Acetonide as Treatment of Exudative Age-Related Macular Degeneration
Author Affiliations & Notes
  • J.B. Jonas
    Faculty of Clinical Medicine Mannheim, University of Heidelberg, Department of Ophthalmology, Mannheim, Germany
  • I. Kreissig
    Faculty of Clinical Medicine Mannheim, University of Heidelberg, Department of Ophthalmology, Mannheim, Germany
  • R.F. Degenring
    Faculty of Clinical Medicine Mannheim, University of Heidelberg, Department of Ophthalmology, Mannheim, Germany
  • Footnotes
    Commercial Relationships  J.B. Jonas, None; I. Kreissig, None; R.F. Degenring, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2003, Vol.44, 973. doi:
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      J.B. Jonas, I. Kreissig, R.F. Degenring; Prospective Comparative Study on Intravitreal Triamcinolone Acetonide as Treatment of Exudative Age-Related Macular Degeneration . Invest. Ophthalmol. Vis. Sci. 2003;44(13):973.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To report on the initial results of a prospective randomized study on the use of intravitreal injection of triamcinolone acetonide as treatment of progressive exudative age-related macular degeneration. Methods: The study included 21 patients presenting with progressive exudative age-related macular degeneration with occult subfoveal neovascularization as shown on fluorescein angiograms. The study group was randomized in a therapeutic group including 9 patients receiving a single intravitreal injection of 25 mg of triamcinolone acetonide, and a control group consisting of 12 patients who did not receive any treatment. Study group and control group did not vary significantly in age (79.3 +/- 6.7 years versus 79.1 +/- 6.2 years; p=0.86) and pre-study visual acuity (0.22 +/- 0.11 versus 0.31 +/- 0.14; p=0.15). Mean follow-up time was 1.1 +/- 0.4 months for the first follow-up examination and 2.0 +/- 0.5 months for the second follow-up examination. Results:. Two months after baseline of the study, mean visual acuity increased in the treated group by 0.04 +/- 0.06. In the same follow-up period, mean visual acuity decreased in the control group by 0.10 +/- 0.22 . The differences between the treated group and the control group were statistically not significant (p>0.05). Conclusions: From a safety monitoring point of view, the preliminary data of this ongoing prospective randomized study do suggest to further continue with a larger number of patients observed for a longer follow-up period.

Keywords: age-related macular degeneration • retinal pigment epithelium • intraocular pressure 
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