Exploratory Study of SAT-001 in Treatment of Pediatric Patient With Myopia
- Conditions
- Children Myopia
- Interventions
- Device: SAT-001(Software as Medical Device)
- Registration Number
- NCT05917041
- Lead Sponsor
- S-Alpha Therapeutics, Inc.
- Brief Summary
The Purpose of this study is to explore the safety and effectiveness of SAT-001, a medical device for the treatment of myopia in pediatric patient with myopia
- Detailed Description
Myopic pediatric prevalence rate come to increase rapidly globally. This is a clinical trial to explore the safety and effectiveness of SAT-001(as a Software as Medical Device) developed for the treatment of myopia through suppressing the progress myopia
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
-
Pediatric patient age 5 to 12 years old at the Screening Visit
-
Diagnosed with myopia as following refractive error via cycloplegic refraction(CR)
- Spherical equivalent (SE) -0.75 D or more and less than -6.00 D in each eye
- Astigmatism of 1.50 D or less in each eye
- Anisometropia of less than 1.00 D
-
The age of birth over 38 weeks
-
Over 2500g of birth weight
-
Best corrected distance visual acuity of 0.2 logMAR or better in each eye at the Screening Visit
-
Intraocular pressure 21 mmHg or less in each eye at the Screening Visit
- Administration of anti-muscarine drugs within 1 month before screening visit
- Current or previous use of multi-focal lenses
- Planning to use or having used Orthokeratology lenses (Ortho-K lenses), Rigid Gas Permeable (RGP) lenses, and other contact lenses to reduce the progression of myopia
- History of atropine use for treatment of myopia within 1 month before screening visit
- Abnormal conditions in cornea, lens, central retina, iris and ciliary bodies or malignant tumors around orbit
- History of manifest strabismus, intermittent strabismus, amblyopia, nystagmus etc. (except for phoria maintaining binocular vision)
- History of ophthalmic surgery, such as eyelid surgery, strabismus surgery, intraocular surgery, or refractive correction surgery (except for epiblepharon surgery)
- Obsessive-compulsive disorder or attention deficit hyperactivity disorder(ADHD)
- Down's syndrome or cerebral palsy
- Participation in another clinical trial within 6 months before screening visit
- History of growth hormone treatment within 1 month before screening visit
- Medically clear to have abnormal range of intellectual development
- Significant systemic diseases such as congenital heart disease, respiratory system disease (except for asthma), endocrine disease or nervous system disease
- Currently taking or having taken antihistamines (tablets, nasal spray, eye drops, etc.) or psychiatric drugs (antidepressants, anti-anxiety medications, etc.) within 30 days before screening visit
- History of injections with histamine release and cholinergic effect within 30 days before screening visit
- Incongruent to participate in this study at the discretion of the investigator
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SAT-001 SAT-001(Software as Medical Device) -
- Primary Outcome Measures
Name Time Method Change in axial length Baseline, 12 weeks, 24 weeks, 36 weeks, 48 weeks Change in cycloplegic Refraction Error Baseline, 24 weeks, 48 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (6)
HanGil Eye Hospital
🇰🇷Incheon, Korea, Republic of
Konkuk University Medical Center
🇰🇷Seoul, Korea, Republic of
Nowon Eulji Medical Center, Eulji University
🇰🇷Seoul, Korea, Republic of
Samsung Medical Center
🇰🇷Seoul, Korea, Republic of
Seoul Asan Medical Center
🇰🇷Seoul, Korea, Republic of
Kangbuk Samsung Medical Center
🇰🇷Seoul, Korea, Republic of