Influence of Hypoxia on Electroretingraphy (ERG) Measurements

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01246024
Recruitment Status : Unknown
Verified November 2010 by University Hospital Tuebingen.
Recruitment status was:  Not yet recruiting
First Posted : November 23, 2010
Last Update Posted : November 23, 2010
Information provided by:
University Hospital Tuebingen

Brief Summary:
To investigate the influence of induced hypoxia on the ERG.

Condition or disease Intervention/treatment Phase
ERG Under Hypoxia Device: ERG Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Study Start Date : February 2011
Estimated Primary Completion Date : April 2011
Estimated Study Completion Date : April 2013

Arm Intervention/treatment
Experimental: Hypoxia Device: ERG
scotopic and photopic ERG

Primary Outcome Measures :
  1. Electroretingraphy Measurements [ Time Frame: 01.02.2011-01.06.2011 ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • healthy subjects

Exclusion Criteria:

  • under 18 and over 80 years, respiratory diseases, cataracta and corneal hazes, myopia more than 6 dpt, hyperopia more than 3 dpt, allergy for any topical anesthetics in ophthalmology, photic epilepsy, asthma bronchiale.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01246024

Contact: Florian Gekeler, Prof. Dr. med. +4970712987461

Centre for Ophthalmology Not yet recruiting
Tübingen, Germany, D-72076
Contact: Andreas Schatz    +70712987461   
Sponsors and Collaborators
University Hospital Tuebingen

Responsible Party: Prof. Dr. med. Florian Gekeler, Centre for Ophthalmology Identifier: NCT01246024     History of Changes
Other Study ID Numbers: THS0001
First Posted: November 23, 2010    Key Record Dates
Last Update Posted: November 23, 2010
Last Verified: November 2010

Additional relevant MeSH terms:
Signs and Symptoms, Respiratory
Signs and Symptoms