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Clinical study of the effect of axial length on the amount of intermittent exotropia in children.

Clinical study of the effect of axial length on the amount of intermittent exotropia in children.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017697
Enrollment
Unknown
Registered
2018-08-10
Start date
2017-02-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

intermittent exotropia

Interventions

Normal axial length group
Abnormal axial length group:axial length

Sponsors

The Second Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 4 to 18 years old and could be well matched with squint angle inspection and axial length measurement; 2. All patients met the basic or separate diagnostic criteria of strong intermittent exotropia (Basic type: The far external angle of deviation is equal to the near one; the differences of the two are less than 8?. Divergence-excess type: The far external angle of deviation is 15? larger than the near one.); 3. The binocular best corrected visual acuity is better than 0.5 and the worst one is better than 0.3. The binocular visual acuity difference is not more than 2 lines (international standard logarithmic visual acuity chart); 4. The degree of equivalent spherical mirror for hyperopia is less than + 3.5 D; 5. The angle of strabismus is between -30?; 6. The patient can be treated with surgery and the condition is good, and the patient is willing to undergo surgical treatment; 7. Normal retinal correspondence; and 8. The patients are followed up for 8 weeks after operation.

Exclusion criteria

Exclusion criteria: 1) Previous history of intraocular surgery, history of strabismus surgery or history of botulinum toxin treatment; 2) Accompanied by anterior segment diseases or fundus diseases; 3) Eye movement dysfunction; 4) Those with paralytic strabismus, vertical dissociative strabismus or nystagmus; 5) Accompanied by monocular or binocular amblyopia; and 6) Those who have poor compliance; 7) With poor compliance with inspection and treatment.

Design outcomes

Primary

MeasureTime frame
postoperative squint angle;

Countries

China

Contacts

Public ContactJiahuan ZHANG

The Second Affiliated Hospital of Dalian Medical University

applw8@outlook.com+86 15004257176

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026