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UHR-OCT and HD-OCT for Preretinal Membranes: ICG Versus Membrane Blue

NCT00437593 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2008-09-23

No results posted yet for this study

Summary

Using the UHR-OCT and HD-OCT to evaluate early postoperative changes in patients with diagnosis preretinal membrane after successfully performed pars-plana vitrectomy and membrane peeling with two different types of dyes.

Conditions

Interventions

PROCEDURE

ppVE, MP, ICG

surgery with ILM staining

PROCEDURE

ppVE, MP, MB

Surgery with ERM staining

Sponsors & Collaborators

  • The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery

    lead OTHER

Principal Investigators

  • Susanne Binder, MD · Ludwig Boltzmann Institue for Retinology and Biomicroscopic Lasersurgery

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2008-05-31
Completion
2008-05-31

Countries

  • Austria

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00437593 on ClinicalTrials.gov