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Recruiting Observational

Patient Preferences on Same-day Bilateral Intravitreal Dexamethasone Injections

NCT06894017 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2025-01-13
Last updated
2025-07-24

Condition(s) studied

Informed ConsentPreference, Patient

Investigational drug(s) / intervention(s)

Ozurdex (dexamethasone) →

Ozurdex (dexamethasone): Intravitreal dexamethasone implant (Ozurdex) given according to the recommendations by the manufacturer.

Study summary

Intravitreal injections with dexamethasone implant (Ozurdex®) provide a reasonable and long-lasting treatment option in the cases of diabetic macular edema, as well as macular edema resulting from retinal vein occlusion and noninfectious posterior uveitis. During the course of these diseases, both eyes may be affected and may need therapy. The treatment burden associated with frequent medical visits associated with treatments in both eyes and follow-ups can be significant for patients and caregivers alike. Same-session bilateral ophthalmic procedures have proven safe and cost-effective, with patients consistently expressing a strong preference for this approach, particularly in the cases of cataract surgery and anti-VEGF injections when given the choice. The safety profile of same-day bilateral dexamethasone injections aligns with those of unilateral injections.

This patient preference study will focus on addressing the practical aspects of same-day bilateral dexamethasone injections from the patients' perspective and aims to explore the impact of personal and socio-economic variables, and the overall perspective of patients on choosing same-day bilateral dexamethasone injections. Understanding and mitigating the challenges patients face can lead to a more patient-friendly and resource-saving approach. Based on the outcomes of this study, considerations may be made to introduce bilateral injections at our department, potentially optimizing patient experience and clinical resources.

The aim of the study is to establish patient preferences regarding the administration of intravitreal dexamethasone implant injections in both eyes on the same day, in the same session and to identify key motivating and limiting factors from the patients' perspective.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria * Having received at least one intravitreal dexamethasone implant in either eye * \>18 years of age * Capacity to comprehend and answer questions in Danish language * Signed informed consent Exclusion criteria • No intravitreal dexamethasone implant received within the last 12 months

Primary outcome measure(s)

  • Preference to bilateral injections — Through study completion, an average of 9 months
    Proportion of patients preferring and not preferring same-day bilateral dexamethasone implant injections

Trial sites (1)

FacilityCityRegionStatus
Department of Ophthalmology, Rigshospitalet Glostrup Municipality Denmark Recruiting
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 NCT06894017 on ClinicalTrials.gov ↗ ← All trials in Denmark