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PERG and mfPERG in Band Atrophy
This study is currently recruiting participants.
Verified by University of Sao Paulo, November 2007
First Received: November 5, 2007   Last Updated: January 28, 2008   History of Changes
Sponsors and Collaborators: University of Sao Paulo
Fundação de Amparo à Pesquisa do Estado de São Paulo
Information provided by: University of Sao Paulo
ClinicalTrials.gov Identifier: NCT00553761
  Purpose

The study is designed to evaluate the ability of pattern electroretinogram (PERG) and multifocal pattern electroretinogram (mfPERG) to measure and identify the pattern of band atrophy of the optic nerve in patients with long standing chiasmal lesions. The hypothesis is that these electrophysiological tests were able to identify this such pattern. The idea is to investigate the ability of the these electrophysiological technics in detecting the neural loss from chiasmal compression and to evaluate the ability of PERG and mfPERG parameters to differentiate between eyes with band atrophy of the optic nerve and healthy eyes.


Condition Intervention
Band Atrophy
Device: Pattern electroretinogram

U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: Pattern Electroretinogram and Multifocal Pattern Electroretinogram For the Detection of Neural Loss in Patients With Permanent Temporal Visual Field Defect From Chiasmal Compression

Further study details as provided by University of Sao Paulo:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 30
Study Start Date: August 2006
Estimated Study Completion Date: February 2008
Intervention Details:
    Device: Pattern electroretinogram
    Full field and hemifield (nasal and temporal) stimulation transient pattern electroretinogram (PERG) were recorded both in patients and controls.
  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Patients with band atrophy from chismal compression and controls

Criteria

Inclusion Criteria:

  1. Visual acuity better than 20/30
  2. Refractive error less 5 spherical diopter and 3 cylinder diopter
  3. Temporal field defect

Exclusion Criteria:

  1. Presence of glaucoma and optic nerve anomalies
  2. Anormal nasal field
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00553761

Contacts
Contact: Leonardo P Cunha, MD 55 11 91465934 leonardo_provetti@yahoo.com.br
Contact: Mário L. R. Monteiro, PhD 55 11 3069 7871 mlrmonteiro@terra.com.br

Locations
Brazil
Universidade de São Paulo Recruiting
São Paulo, Brazil, 05403-000
Contact: Leonardo P Cunha, MD     55 11 91465934     leonardo_provetti@yahoo.com.br    
Principal Investigator: Leonardo P Cunha, MD            
Sponsors and Collaborators
University of Sao Paulo
Fundação de Amparo à Pesquisa do Estado de São Paulo
Investigators
Study Chair: Mário Luiz R Monteiro, PhD Universidade de São Paulo
  More Information

Additional Information:
No publications provided by University of Sao Paulo

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Responsible Party: University of Sao Paulo ( Mario Luiz Ribeiro Monteiro/University of Sao Paulo )
Study ID Numbers: 654/06, FAPESP 06/61549-6; 07/54142-0)
Study First Received: November 5, 2007
Last Updated: January 28, 2008
ClinicalTrials.gov Identifier: NCT00553761     History of Changes
Health Authority: Brazil: National Committee of Ethics in Research

Keywords provided by University of Sao Paulo:
Band atrophy
Pattern electroretinogram
Chiasmal compression
Neural loss
Electrophysiological tests

Study placed in the following topic categories:
Pathological Conditions, Anatomical
Atrophy
Scotoma

Additional relevant MeSH terms:
Pathological Conditions, Anatomical
Atrophy

ClinicalTrials.gov processed this record on May 06, 2009