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Clinical Trials in Italy / NCT06819631
Starting soon Observational

Characterization of Subjective Discomfort in Patients With Tear Dysfunction

NCT06819631 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Phase
Observational
Started
2025-03
Last updated
2025-02-11

Condition(s) studied

Dry Eye Disease

Study summary

Characterization of subjective discomfort/pain in patients with ocular surface dysfunction in association with clinical and laboratory parameters, for a better understanding of the underlying pathogenic mechanisms.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * adult patients with suspected or diagnosed DED Exclusion Criteria: * nothing

Primary outcome measure(s)

  • Discomfort in subjects affected by Dry Eye Disease (DED) — Baseline (enrollment visit)
    Assessment of discomfort with Ocular Surface Disease Index (OSDI) and Dry Eye Questionaire-5 (DEQ-5)
  • Pain in subjects affected by Dry Eye Disease (DED) — Baseline (enrollment visit)
    Assessment of pain with Visual Analogue Scale (VAS) and Numeric Rating Scale (NRS)

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Italy

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06819631 on ClinicalTrials.gov ↗ ← All trials in Italy