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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01422525
Other study ID # OCT-TET
Secondary ID
Status Terminated
Phase N/A
First received August 21, 2011
Last updated December 1, 2014
Start date November 2011

Study information

Verified date December 2014
Source University Eye Hospital, Würzburg
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

At present, trabeculectomy is the most common performed and effective surgical method of filtration surgery for patients with medically uncontrolled glaucoma.

The aim of this prospective observational case study is to determine changes of the peripapillary retinal nerve fiber layer thickness using spectral domain optical coherence tomography in patients with glaucoma after surgical reduction of intraocular pressure.


Description:

Baseline and postoperative measurement of the peripapillary retinal nerve fiber layer (RNFL) thickness will be performed using the following spectral domain optical coherence tomography (OCT): Cirrus™ HD-OCT (Carl Zeiss Meditec) and Spectralis® Heidelberg-Engineering.

The main outcome measures will be changes in overall and quadrant RNFL thickness with respect to reduction in intraocular pressure (IOP), correlation between RNFL thickness and alteration in visual field and predictive factors of postoperative IOP-reduction and changes of RNFL thickness.


Recruitment information / eligibility

Status Terminated
Enrollment 12
Est. completion date
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- primary or secondary open angle glaucoma

- target intraocular pressure under medical treatment was not reached

- progression of visual loss

- best corrected visual acuity of 20/100 or more

- spherical equivalent refraction of -8.0 to +4.0 D

- perimetry: less than 20% false positive answers

Exclusion Criteria:

- primary or secondary angle closure glaucoma

- congenital glaucoma

- normal tension glaucoma

- neovascular glaucoma

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Procedure:
spectral domain optical coherence tomography
RNFL thickness measurement using spectral domain optical coherence tomography at baseline, 1, 3 and 6 months postoperatively.

Locations

Country Name City State
Germany University Eye Hospital Wuerzburg Wuerzburg Bavaria

Sponsors (1)

Lead Sponsor Collaborator
University Eye Hospital, Würzburg

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of retinal nerve fiber layer thickness study was terminated 6 months No
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