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Generalized Visual Field Contraction or ConstrictionNCT01843582

A Study to Determine the Location of the Blind Spot and the Macula-disc Centre Distance on a Fundus Photograph

An observational study of Generalized Visual Field Contraction or Constriction, run by Turku University Hospital at 1 site in Finland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study is aimed to develop a new reaction-time based method for examining the visual field and to study the effect of refractive error on the magnification of a fundus photograph in order to evaluate the true size of a retinal feature. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
17 participants
Where
1 siteFinland
Study dates
May 2013to Nov 2014
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Healthy volunteers

Who may be able to join

  • No disease that effect the fundus photograph or visual field

Who cannot join

  • any disease that effects the fundus photograph or visual field

Trial locations and contacts

1 site in 1 country.

Finland1 site
  • Turku University Hospital

    Turku, 20521

Other trials in Finland

About this study

Official title: A Study to Develop Both a Novel Method for Evaluating the True Size of a Retinal Object on Fundus Photographs and a New Reaction-time Based Method for Studying the Visual Field on Healthy Volunteers

The study is aimed to develop a new reaction-time based method for examining the visual field and to study the effect of refractive error on the magnification of a fundus photograph in order to evaluate the true size of a retinal feature.

Keywords
Keyword: blind spot
Medical subject headings
Constriction, Pathologic

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Macula-disc centre distance

    Measurement is done on a fundus photograph (one visit and one examination for each patient)

    Measured: one measurement at the start of the study

Secondary outcomes (1)
  1. Location of the blind spot

    The location of the blind spot is screened using Octopus custom made visual field program at the one visit (one visit and one study for each patient) and a novel reaction-time based visual field device.

    Measured: one measurement at the start of the study

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2013 (estimated)
  2. Study startMay 2013
  3. Primary completionAug 2014
  4. Study completionNov 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
17 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT01843582
Sponsor's protocol ID
T81/2012
Status last verified
May 2013
First submitted
26 Apr 2013
Last updated
27 Feb 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Generalized Visual Field Contraction or Constriction, run by Turku University Hospital at 1 site in Finland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Feb 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Macula-disc centre distance (time frame: one measurement at the start of the study). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Feb 2015.

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