Prism Adaptation in Symptomatic Esophoria - Effect of Shorter Time Intervals and Surgical Outcomes Based on Prism Adaptation
Recruiting
N/A
Interventional Study
Esophoria
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- Rigshospitalet, Denmark · Other
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About This Trial
This study is a prospective randomized study aiming to investigate the effect of prism adaptation before surgery for symptomatic esophoria on the number of reoperations, the occurrence of over- and under-correction after the first surgery, and symptom resolution. Additionally, we aim to define the optimal duration of prism adaptation.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Patients with symptomatic esophoria who meet one or more of the following criteria:
* Double vision
* Asthenopia (eye strain)
* Headaches related to esophoria
* Worsening of symptoms during fatigue, sleep deprivation, reading, illness, or alcohol consumption.
Exclusion Criteri…
Contacts