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Macular EdemaNCT00791726

Microperimetry in Macular Edema

An observational study of Macular Edema and Uveitis, run by St. Franziskus Hospital at 1 site in Germany.

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

In uveitic patients with fluorescein angiographically proven macular edema, a fundus related microperimetry is performed and results are correlated with foveal thickness as measured with optical coherence tomography (OCT). Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Macular Edema, Uveitis
How many people
30 participants
Where
1 siteGermany
Study dates
Nov 2008to not given
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 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with noninfectious uveitis, macular edema

Who may be able to join

  • Patients with noninfectious uveitis, macular edema

Who cannot join

  • Pregnancy, fluorescein allergy

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Department of Ophthalmology at St Franziskus Hospital

    Münster, Northrhine-Westfalia, 48145

Other trials in Germany

About this study

Official title: Place of Fundus-related Microperimetry in Uveitic Macular Edema

In uveitic patients with fluorescein angiographically proven macular edema, a fundus related microperimetry is performed and results are correlated with foveal thickness as measured with optical coherence tomography (OCT).

Keywords
microperimetry, macular edema, uveitis, Retinal sensitivity as measured with fundus related microperimetry
Medical subject headings
Macular Edema, Uveitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00791726
Study groupRoleWhat they receive
1Patients with noninfectious uveitis and macular edema

Timeline

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

  1. First posted14 Nov 2008 (estimated)
  2. Study startNov 2008

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
Cohort
Time perspective
Cross-sectional
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00791726
Sponsor's protocol ID
2008-448-f-S
Status last verified
Mar 2011
First submitted
13 Nov 2008
Last updated
21 Jul 2011
Results posted
No
Data monitoring committee
No

Publications

  • Roesel M, Heimes B, Heinz C, Henschel A, Spital G, Heiligenhaus A. Comparison of retinal thickness and fundus-related microperimetry with visual acuity in uveitic macular oedema. Acta Ophthalmol. 2011 Sep;89(6):533-7. doi: 10.1111/j.1755-3768.2009.01750.x. Epub 2009 Dec 9.

    PubMed 20003108

Questions about this trial

What is this clinical trial studying?

An observational study of Macular Edema and Uveitis, run by St. Franziskus Hospital at 1 site in Germany.

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 21 Jul 2011. 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 Germany. 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.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00791726, which also lists 1 linked publication.

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 21 Jul 2011; AzTrials last refreshed its copy on 29 Oct 2026.

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