Trials / Terminated
TerminatedNCT02767856
Regimens of Intermittent Occlusion Therapy for Amblyopia in Children
Intense vs Standard Regimens of Intermittent Occlusion Therapy for Unilateral Moderate Amblyopia in Children
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Salus University · Academic / Other
- Sex
- All
- Age
- 3 Years – 8 Years
- Healthy volunteers
- Accepted
Summary
This study is designed to answer the question: What if the Intermittent Occlusion (IO-therapy) glasses were prescribed all day (12-hours) in which the total time of treatment only took 4 weeks instead of the current treatment time (4 hours) in which it takes 12 weeks? Children aged 3- to 8-years with untreated moderate unilateral amblyopia will be enrolled and randomized into 2 groups: 1) Intense 12-hour IO-therapy Group for 4 weeks treatment; or 2) Standard 4-hour IO-therapy glasses Group for 12 weeks treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | IO-therapy Glasses |
Timeline
- Start date
- 2016-09-01
- Primary completion
- 2021-05-30
- Completion
- 2021-05-30
- First posted
- 2016-05-10
- Last updated
- 2022-07-25
- Results posted
- 2022-07-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02767856. Inclusion in this directory is not an endorsement.