AzTrials
AzTrials

Anterior UveitisNCT01156285

Acute Anterior Uveitis: Psychic Burden and Pain

An observational study of Anterior Uveitis, run by Hospital Hietzing at 2 sites in Austria.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Acute anterior uveitis (AU) is a common reason for attendance at ophthalmic outpatient clinics. The painfulness and the fear of a transient or even persistent loss of vision may markedly reduce the individual's subjective well-being and pose a psychological burden. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Anterior Uveitis
What is being tested?
Filling in a patient questionnaire
How many people
35 participants
Where
2 sitesAustria
Study dates
May 2010to Jun 2012
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 acute attack of anterior uveitis

Who may be able to join

  • Acute attack of anterior uveitis

Who cannot join

  • Other forms of uveitis
  • Chronic anterior uveitis
  • Therapy started

Trial locations and contacts

2 sites in 1 country.

Austria2 sites, 2 recruiting
  • Department of Ophthalmology, Medical University Graz

    Graz, Styria

    Andreas Wedrich, MD, Prof., 43-316-385 ext. 2394

    Andreas Wedrich, MD, Prof

    Not yet recruiting
  • Department of Ophthalmology, Hietzing Hospital

    Vienna, State of Vienna, 1130

    Saskia M Maca, MD

    Recruiting

Other trials in Austria

About this study

Acute anterior uveitis (AU) is a common reason for attendance at ophthalmic outpatient clinics. The painfulness and the fear of a transient or even persistent loss of vision may markedly reduce the individual's subjective well-being and pose a psychological burden.

This study will test the hypothesis that during an attack of AU the patient experiences a marked reduction in psychological and physical well-being.

Prospective, hospital-based epidemiologic study using a patient questionnaire with standardized psychological tests and a pain scale.

Being tested
Filling in a patient questionnaire
Medical subject headings
Uveitis, Anterior

What participants receive

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

  • Filling in a patient questionnaireOther

    Filling in a patient questionnaire

Study groups in NCT01156285
Study groupRoleWhat they receive
AAUpatient with acute attack of anterior uveitis
Receives: Other: Filling in a patient questionnaire

Timeline

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

  1. First posted2 Jul 2010 (estimated)
  2. Study startMay 2010
  3. Study completionJun 2012 (estimated)

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
Prospective
Enrolment
35 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01156285
Sponsor's protocol ID
MAC110
Status last verified
Nov 2011
First submitted
1 Jul 2010
Last updated
29 Nov 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Anterior Uveitis, run by Hospital Hietzing at 2 sites in Austria.

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 3 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: status not confirmed, as of the sponsor's last update on 29 Nov 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Austria. 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?

Results are not available in the source record.

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

Contact Saskia M Maca, MD (+43-1-80110 ext. 2266, Saskia.Maca@wienkav.at), or a site near the patient. AzTrials does not enrol participants or take referrals.

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 29 Nov 2011.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in