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NCT Number: NCT06894017

Patient Preferences on Same-day Bilateral Intravitreal Dexamethasone Injections

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Ophthalmology, Rigshospitalet

Glostrup Municipality, 2600, Denmark

Location status: Recruiting

Location contact

Lena Michelle Mørup Andersen, MScN

CONTACT

[email protected]

+4538634700

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Ozurdex (dexamethasone)

Drug

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

Other names: Intravitreal dexamethasone implant

Primary outcomes

  1. Preference to bilateral injections

    Time frame: Through study completion, an average of 9 months

    Proportion of patients preferring and not preferring same-day bilateral dexamethasone implant injections

Secondary outcomes

  1. Reasons

    Time frame: Through study completion, an average of 9 months

    For preferring or not preferring same-day bilateral injections from the patient's perspective

  2. Differences in patient characteristics

    Time frame: Through study completion, an average of 9 months

    Between preference groups in: Age, Sex, Previous injection count, Indication for intravitreal treatment (medical diagnosis), Complications of previous treatments, Ocular comorbidity (e.g. glaucoma, cataract, previous retinal detachment etc.), Systemic comorbidity

  3. Differences in socio-economic variables between preference groups

    Time frame: Through study completion, an average of 9 months

    As in: Need for caregivers, Means of transportation, Transport distance, Active vs retired, Highest education level

Study contacts

Contact information is provided by the study sponsor or research team.

Lena Michelle Mørup Andersen, MScN

CONTACT

[email protected]

+4538634700

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Mar 25, 2025
Registry last updated
Jul 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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