NCT01732042

Completed

Retinal Venous Pressure (RVP) in Normals

University Hospital, Basel, Switzerland Source

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Other study identifiers

Sponsor study identifier

USB-2011-326

Study Type

observational

Actual enrollment (reported)

200

Locations

1 country

Sites

1

Timeline

Study Start

November 2011

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

June 2013

Actual (reported)

Study Completion

December 2013

Actual (reported)

Brief Summary

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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 200 participants
Study completion date: December 2013
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
November 2011
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
October 24, 2012
Actual (reported)
First Posted
November 22, 2012
Actual (reported)
Primary Completion
June 2013
Actual (reported)
Study Completion
December 2013
Actual (reported)

Last Updated: December 11, 2013
Status Verified: December 2013
Last Update Submitted: December 10, 2013

Conditions

Healthy

Keywords

retinal venous pressure

Outcome Measures

Primary Outcomes (1)

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

Eligibility Criteria

Age18 Years - 80 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

healthy volunteers

You may qualify if:

healthy

You may not qualify if:

Sponsors & Collaborators

University Hospital, Basel, Switzerland
Otherlead

Study Sites (1)

University of Basel, Dept. of Ophthalmology

Basel, 4031, Switzerland

Study Officials

Josef Flammer, MD
University of Basel, Dept. of Ophthalmology
STUDY DIRECTOR

Enrollment

200 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

October 24, 2012

First Posted

November 22, 2012

Study Start

November 2011

Date type not reported

This date has not been verified as actual or estimated.

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Recruiting

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

Contact the study team to confirm eligibility.

Primary Completion

June 2013

Actual (reported)

Study Completion

December 2013

Actual (reported)

Last Updated

December 11, 2013

Record last verified: 2013-12

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01732042
Data provider: ClinicalTrials.gov
Source updated: 2013-12-11
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:20:01 UTC

Locations

CH(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations