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Vision Therapy Versus Prism Treatment in Small-angle Acute Acquired Concomitant Esotropia

Accommodation and Vergence Exercises Versus Prism Treatment for Small-angle Acute Acquired Concomitant Esotropia

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06622044
Enrollment
100
Registered
2024-10-01
Start date
2024-09-07
Completion date
2026-12-07
Last updated
2025-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esotropia

Keywords

Vision Therapy, Acute Acquired Concomitant Esotropia

Brief summary

This is a single-center, randomized controlled clinical trial to compare the effectiveness of vision therapy and prism wearing for the treatment of small-angle acute acquired concomitant esotropia.

Detailed description

Acute acquired concomitant esotropia (AACE) belongs to the category of concomitant strabismus. It is characterized by sudden onset, often accompanied by diplopia, and no change in the strabismus angle of each eye position. In recent years, with the increase in the use of smartphones and other screen devices, the incidence of AACE has been on the rise. Commonly used treatments in clinical practice include surgical treatment, botulinum toxin injection into the medial rectus muscle, and prism treatment. Patients with large-angle esotropia generally require surgical intervention to fundamentally correct patients eye positions and eliminate diplopia. However, surgical treatment requires waiting for six months in order to performed after the strabismus degree is stable. There are also risks of intraoperative trauma and secondary surgery. Patients with early and small-angle esotropia often choose prism treatment. The principle of prism treatment is light refraction. After light is refracted through a prism, it falls on the fovea of the strabismic eye, eliminating diplopia. In the treatment of AACE, the main target population of prisms is patients with mild strabismus (the strabismus angle is usually less than 25 PD). Wearing prisms can eliminate diplopia and relieve related symptoms, but it does not really correct the strabismus problem. The high incidence of AACE is related to excessive close work and use of electronic products. Excessive close eye use can lead to accommodative dysfunction. Studies have found that AACE patients have abnormal accommodative function. The accommodative function of AACE patients is weaker than normal, and the accommodation convergence to accommodation (AC/A) ratio is higher than normal. During clinical diagnosis and treatment, the accommodative function of AACE patients was examined and it was found that there was indeed abnormal accommodative function. Based on scientific research findings and the actual basis of clinical practice, improving accommodative function through accommodative training may be a good treatment option for early and small-angle AACE patients. However, existing studies have not fully explored the effectiveness and safety of accommodative exercise in the treatment of small-angle AACE, and there has been no study comparing the therapeutic outcomes of accommodative training and prism treatment on small-angle AACE. In order to better guide clinical practice, we conducted a randomized controlled study to objectively evaluate and compare the therapeutic effects of accommodative training and prism therapy on AACE. It is expected that the research results will provide more treatment options for AACE patients and provide important guidance for clinical selection of appropriate methods to treat small-angle AACE.

Interventions

OTHERVision therapy group

accommodation and vergence exercise

OTHERPrism

wearing prism glasses

Sponsors

Eye & ENT Hospital of Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
10 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 10-40 years (including 10 years and 40 years); 2. Best-corrected visual acuity no worse than 20/20 for both eyes; 3. Deviation angle less than 15 prism diopters (including 15 prism diopters);

Exclusion criteria

1. Organic eye diseases; 2. Lesions of the brain; 3. Receiving esotropia therapy(including surgery and prism treatment) 4. Devation angle reducing more than 10 prism diopters after refractive correction

Design outcomes

Primary

MeasureTime frameDescription
Change in deviation angle at distance and near1 weeks, 4weeks, 12 weeks, 24 weeksthe deviation angle measured using the alternate prism cover test

Secondary

MeasureTime frameDescription
Changes in stereopsis1 weeks, 4weeks, 12 weeks, 24 weeksNear and far stereopsis measured with Randot Stereotest pattern
Changes in accommodation facility1 weeks, 4weeks, 12 weeks, 24 weeksAccommodation facility measured with accommodative flipper
Changes in accommodation function1 weeks, 4weeks, 12 weeks, 24 weeksAccommodation function including accommodation amplitude, accommodation response, positive relarive accommodation, and negative relative accommodation measured with phoropter
Change in accommodation convergence to accommodation(AC/A) ratio1 weeks, 4weeks, 12 weeks, 24 weeksAC/A ratio measured with synoptophore

Countries

China

Contacts

Primary ContactWen Wen, MD, PhD
wenweneye@126.com+86 (21) 3423 3133
Backup ContactShuyang Guo, MD
m15880091363@163.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026