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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01299129
Other study ID # 070/2009
Secondary ID
Status Completed
Phase N/A
First received February 17, 2011
Last updated December 24, 2011
Start date June 2009
Est. completion date June 2011

Study information

Verified date December 2011
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority Austria: Federal Ministry for Health and Women
Study type Observational

Clinical Trial Summary

Purpose:

To evaluate the effect of intravitreal triamcinolone acetonide (IVTA) on uveitis-associated cystoid macular edema (CME) using high resolution optical coherence tomography (SDOCT) in conjunction with thorough visual function testing.

Methods:

28 patients with uveitis-associated CME were examined before intravitreal triamcinolone injection (IVTA) (v1) and at day 1 (v2), week 1 (v3) and month 1 (v4) after injection. Retinal anatomy was evaluated using Cirrus HD-OCT (Carl Zeiss Meditec). Visual function testing consisted of assessing ETDRS distance visual acuity (VA), reading acuity and reading speed using a standardized German-language test (Radner Reading charts), contrast sensitivity using Pelli-Robson Contrast Sensitivity charts and fundus-controlled microperimetry using the MP-1 Microperimeter (Nidek). Here we utilized a cartesian grid consisting of a central locus and three concentric box-shaped stimulation areas. The changes of retinal anatomy over time were compared to the respective outcome of visual function.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- intraocular inflammation

- able to read

- > 18 years old

Exclusion Criteria:

- cataract

- amblyopia

- dyslexia

- already applicated intravitreal triamcinolone for current cystoid macular edema

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Austria Medical University Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

See also
  Status Clinical Trial Phase
Recruiting NCT05608837 - Multicenter Study on the Efficacy and Safety of OCS-01 in Subjects With Uveitis Related and Post Surgical Macular Edema Phase 2
Completed NCT01564108 - The LIMO Study, Lucentis for Treatment of Uveitic Patients With Refractory Cystoid Macular Oedema Phase 2