Optimizing Patient's Comfort During Scleral Indentation
- Sponsor
- University of Alberta
- Study ID
- NCT06683209
- Status
- Not Yet Recruiting
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Conditions
- Pain
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Accepted
Interventions
- Schocket scleral depressor — DIAGNOSTIC_TESTUse of this instrument to examine one eye
- Josephberg-Besser — DIAGNOSTIC_TESTUse of this instrument to examine one eye
- Cotton tip applicator — DIAGNOSTIC_TESTUse of this instrument to examine one eye
Study Details
The scleral depression exam is an important routine technique for evaluating the retinal periphery for various reasons. During this examination, an instrument is used to bring the anterior part of the retina into the physician's field of view. The downside of this technique is the discomfort it may cause the patient. Different instruments can be used to depress the sclera. The objective of this research is to compare three commonly used scleral depressors based on their performance for the ophthalmologist and the discomfort they subjectively induce in patients. Patients will be randomly allocated to one of three examination groups: Group A: One eye examined with the Schocket scleral depressor, the other eye with the Josephberg-Besser scleral depressor. Group B: One eye examined with the Schocket scleral depressor, the other eye with the cotton-tip applicator. Group C: One eye examined with the cotton-tip applicator, the other eye with the Josephberg-Besser scleral depressor.
Key Dates
- First listed
- Nov 12, 2024
- Start date
- Jul 1, 2026
- Status verified
- Jul 2025
- Primary completion
- Jul 30, 2026
- Completion
- Jul 30, 2026
Study Design
- Enrollment
- 75 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Active Comparator: Group AOne eye examined with the Schocket scleral depressor, the other eye with the Josephberg-Besser scleral depressor
- Active Comparator: Group BOne eye examined with the Schocket scleral depressor, the other eye with the cotton tip applicator
- Active Comparator: Group COne eye examined with the cotton tip applicator, the other eye with the Josephberg-Besser scleral depressor
Primary Outcome Measure
Pain scale [ Time Frame: Once, directly after completing the scleral depressed examination, on the same day of inclusion in the study. ]
Central Contacts
- Mathieu Carrière, MD, FRCSC(780) 448-1801
- Parampal Grewal(780) 448-1801
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