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OpenTrials
Completed

NCT Number: NCT01732042

Retinal Venous Pressure (RVP) in Normals

Determinate the standard values of the retinal venous pressure in a cohort of healthy subjects.

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Key information

Conditions

Healthy

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Basel, Dept. of Ophthalmology

Basel, 4031, Switzerland

About this study

The retinal venous pressure (RVP) is an increasingly important dimension in the clinical assessment of retinal blood flow.

In literature only very few and also divergent data on the retinal venous pressure in healthy volunteers are described. A normal value study will provide us with an up-to-date database.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • healthy

Exclusion criteria

  • eye diseases
  • systemic diseases
  • term medication (except contraceptives)
  • pregnancy
  • allergies to the ingredients Alcaine, Tropicamide and Phenylephrine

Treatment and study plan

Primary outcomes

  1. Retinal venous pressure

    Time frame: 1 hour

    Quantification of the retinal venous pressure as a standard value in a cohort of healthy volunteers

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Nov 22, 2012
Registry last updated
Dec 11, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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