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Influence of Hypoxia on Electroretingraphy (ERG) Measurements

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ClinicalTrials.gov 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
Sponsor:
Information provided by:

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

Condition or disease Intervention/treatment
ERG Under Hypoxia Device: ERG

Study Design

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
Arms and Interventions

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


Outcome Measures

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

Eligibility Criteria

Information from the National Library of Medicine

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

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.
Contacts and Locations

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 ClinicalTrials.gov identifier (NCT number): NCT01246024


Contacts
Contact: Florian Gekeler, Prof. Dr. med. +4970712987461 fgekeler@googlemail.com

Locations
Germany
Centre for Ophthalmology Not yet recruiting
Tübingen, Germany, D-72076
Contact: Andreas Schatz    +70712987461    schatzweb@gmail.com   
Sponsors and Collaborators
University Hospital Tuebingen
More Information

Responsible Party: Prof. Dr. med. Florian Gekeler, Centre for Ophthalmology
ClinicalTrials.gov 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:
Hypoxia
Signs and Symptoms, Respiratory
Signs and Symptoms