Monitored Controlled Intermittent Alternate Occlusion (CIAO) Therapy for Intermittent Exotropia

Intermittent Exotropia Clinical Trial

Official title:

A Clinical Trial of Observation Versus Controlled Intermittent Alternate Occlusion (CIAO) Therapy for Intermittent Exotropia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02902887
• Other study ID #: HJW1601
• Status: Recruiting
• Phase: N/A
• Start date: August 2016
• Est. completion date: May 2021

Study information

• Verified date: April 2019
• Source: Salus University
• Contact: Jingyun Wang, PhD
• Phone: 215-780-1376
• Email: jwang[@]salus.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study presents an opportunity to understand a novel, previously unreported controlled intermittent alternate occlusion (CIAO) therapy glasses, which may improve the control of Intermittent exotropia (IXT).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: May 2021
• Est. primary completion date: May 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 3 Years to 11 Years

Eligibility

Inclusion Criteria:

The following criteria must be met for the patient to be enrolled in the study:

1. Age 3 to 11 years old

2. Intermittent exotropia (manifest deviation) meeting all of the following criteria:

• Intermittent exotropia at distance OR constant exotropia at distance and either intermittent exotropia or exophoria at near

• Exodeviation at least 10PD at distance OR 15PD at near measured by prism and alternate cover test (PACT)

3. No previous surgical or non-surgical treatment for IXT (other than refractive correction)

4. Visual acuity in the worse eye 20/40 (0.3 logMAR) or better on ATS HOTV for ages 3 - 5 and 20/25 (0.1 logMAR) or better on ATS HOTV for ages 6 - 11

5. No hyperopia greater than +3.50 D spherical equivalent in either eye

6. No myopia greater than -6.00 D spherical equivalent in either eye

7. Patients must be wearing refractive correction (spectacles or contact lenses) for at least one week if refractive error (based on cycloplegic refraction performed within 6 months) meets any of the following:

• Myopia > -0.50 D spherical equivalent in either eye

• Anisometropia > 1.00 D spherical equivalent

• Astigmatism in either eye > 2.00 D if = 5 years old and > 1.50 D if > 5 years old

Refractive correction for patients meeting the above refractive error criteria must meet the following guidelines:

• Anisometropia spherical equivalent must be within 0.25D of the full anisometropic difference correction

• Astigmatism cylinder must be within 0.25D of full correction and axis must be within 5 degrees of full correction.

• For hyperopia, the spherical component can be reduced at investigator discretion provided the reduction is symmetrical. Prescribing any refractive correction to yield lenses that are more myopic than -0.50 D spherical equivalent (SE) is considered deliberate overminus and is not allowed at enrollment. However, prescribing no correction or prescribing less than the full cycloplegic hyperopic correction (i.e., prescribing reduced plus) is not considered the same as overminusing for this protocol and is allowed because most patients without IXT but with hyperopic SE refractions in this range would not typically be prescribed a refractive correction.

• For myopia, the intent is to fully correct, but the spherical component can be undercorrected by investigator discretion provided the reduction is symmetrical and results in no more than -0.50 D SE residual (i.e., uncorrected) myopia. Prescribing a correction that yields more than 0.50 D more minus SE than the cycloplegic refraction SE is considered deliberate overminus and is not allowed at enrollment.

Note that the refractive correction guidelines and the requirement to wear refractive correction for at least one week apply not only to patients who require refractive correction under the above criteria but also to any other patient who is wearing refractive correction.

8. No atropine use within the last week

9. Gestational age > 34 weeks and birth weight > 1500 grams

10. Patient and/or parent is willing to accept randomization to either observation or CIAO therapy.

11. Parent has a phone (or access to phone) and is willing to be contacted

Exclusion Criteria:

1. Only phoria at both distance and near

2. Prior non-surgical treatment for IXT other than refractive correction (e.g., vergence therapy, occlusion, vision therapy/orthoptics, or deliberate over-minus with spectacles more than 0.50D)

3. Previous amblyopia treatment other than refractive correction within 1 year

4. Vision therapy/orthoptics for any reason within the last year

5. Interocular visual acuity difference more than 0.2 logMAR (2 lines on ATS HOTV for patients 3 to < 7 years old or 10 letters on E-ETDRS for patients = 7 years old)

6. Investigator planning to initiate amblyopia treatment

Related Conditions & MeSH terms

• Exotropia
• Intermittent Exotropia

Intervention

Device:
• Controlled Intermittent Alternate Occlusion (CIAO ) glasses
Monitored CIAO therapy glasses

Locations

Country	Name	City	State
United States	Salus University	Elkins Park	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Salus University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Control of the exodeviation assessment (scaled 1-5)	Intermittent Exotropia Control Scale (1-5) 5 = Constant exotropia 4 = Exotropia > 50% of the 30-second period before dissociation 3 = Exotropia < 50% of the 30-second period before dissociation 2 = No exotropia unless dissociated, recovers in > 5 seconds; 1 = No exotropia unless dissociated, recovers in 1-5 seconds 0 = No exotropia unless dissociated, recovers in < 1 second (phoria)	3-month