NCT01732042CompletedNot Applicable
Retinal Venous Pressure (RVP) in Normals
University Hospital, Basel, Switzerland1 site in 1 country200 target enrollmentStarted: November 2011Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- Retinal venous pressure
Study Overview
Brief Summary
Determinate the standard values of the retinal venous pressure in a cohort of healthy subjects.
Detailed Description
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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Not provided
Exclusion Criteria
- •eye diseases
- •systemic diseases
- •term medication (except contraceptives)
- •pregnancy
- •allergies to the ingredients Alcaine, Tropicamide and Phenylephrine
Outcomes
Primary Outcomes
Retinal venous pressure
Time Frame: 1 hour
Quantification of the retinal venous pressure as a standard value in a cohort of healthy volunteers
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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