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Acute and Chronic Inflammatory Disease, Lifestyle and Treatment Response (ACID LTR)

W

Wroclaw Medical University

Status

Enrolling

Conditions

Uveitis

Treatments

Other: Surveillance card

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Acute and chronic inflammatory eye diseases are difficult to diagnose and maintain quiescent with therapy. Proposed study is aimed to find on the one hand, novel factors for recurrence of the disease or remission of inflammation and evaluation of the impact of lifestyle and known factors on the other.

Each patient is treated in accordance to the best of medical knowledge and guidelines for each disease.

This prospective cohort study will enroll uveitic patients to the steroid only group (SG), combined (steroid and adjuvant drug) group (CG) or bilogic therapy group (BTG).

At baseline, patient data are recorded using patient-reported outcome measures and clinical assessments (ophthalomology) on disease activity (clinical scales), quality of life, and lifestyle together with registry data on comorbidity and medication. During follow-up evaluation of a successful treatment outcome response will be based on clinical scales and most frequently used primary endpoints; the major outcome of the analyses will be to detect differences in treatment outcome between patients in different treatment group.

Enrollment

300 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • new diagnosis of uni or bilateral uveitis
  • recurrence of the diagnosed previously uni or bilateral uveitis

Exclusion criteria

  • not mentally able to reply the questionnaire

Trial design

300 participants in 3 patient groups

steroid only group (SG)
Treatment:
Other: Surveillance card
combined (steroid and adjuvant drug) group (CG)
Treatment:
Other: Surveillance card
bilogic therapy group (BTG)
Treatment:
Other: Surveillance card

Trial contacts and locations

1

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Central trial contact

Joanna Przeździecka-Dołyk, PhD

Data sourced from clinicaltrials.gov

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